Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
CTT/-
Location

Chromosome 1:201331100-201331102 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 5868

This variation has 28 HGVS names - click the plus to show

1:g.201331100_201331102delCTT
ENST00000491504.1:n.1867_1869delAAG
ENST00000367318.5:c.628_630delAAG
ENSP00000356287.5:p.Lys210del
ENST00000458432.2:c.655_657delAAG
ENSP00000387874.2:p.Lys219del
ENST00000460780.1:n.951_953delAAG
ENST00000367317.4:c.628_630delAAG
ENSP00000356286.4:p.Lys210del
ENST00000367315.2:c.619_621delAAG
ENSP00000356284.2:p.Lys207del
ENST00000360372.4:c.613_615delAAG
ENSP00000353535.4:p.Lys205del
ENST00000367322.1:c.619_621delAAG
ENSP00000356291.1:p.Lys207del
ENST00000421663.2:c.637_639delAAG
ENSP00000404134.2:p.Lys213del
ENST00000509001.1:c.628_630delAAG
ENSP00000422031.1:p.Lys210del
ENST00000476888.1:n.113_115delAAG
ENST00000438742.1:c.610_612delAAG
ENSP00000414036.1:p.Lys204del
ENST00000367320.2:c.529_531delAAG
ENSP00000356289.2:p.Lys177del
ENST00000515042.1:n.554_556delAAG
ENST00000236918.7:c.643_645delAAG
ENSP00000236918.7:p.Lys215del
ENST00000479297.1:n.344_346delAAG

Variation displays