Canonical Allele Identifier: CA1618519355
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944449_29944452delinsCTGG , CM000668.2:g.29944449_29944452delinsCTGG GRCh38
NC_000006.11:g.29912226_29912229delinsCTGG , CM000668.1:g.29912226_29912229delinsCTGG GRCh37
NC_000006.10:g.30020205_30020208delinsCTGG NCBI36
NG_029217.2:g.6985_6988delinsCTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.895+52_895+55delinsCTGG ENSP00000492789.2:n.895+52_895+55delinsCT...
ENST00000706892.1:n.1801_1804delinsCTGG
ENST00000706893.1:c.896-17_896-14delinsCTGG ENSP00000516609.1:n.896-17_896-14delinsCT...
ENST00000706894.1:c.896-51_896-48delinsCTGG ENSP00000516610.1:n.896-51_896-48delinsCT...
ENST00000706895.1:n.1223_1226delinsCTGG
ENST00000706896.1:n.1750-51_1750-48delinsCTGG
ENST00000706897.1:n.1172-51_1172-48delinsCTGG
ENST00000706898.1:c.896-51_896-48delinsCTGG ENSP00000516611.1:n.896-51_896-48delinsCT...
ENST00000706899.1:n.1750-51_1750-48delinsCTGG
ENST00000706900.1:c.812-51_812-48delinsCTGG ENSP00000516617.1:n.812-51_812-48delinsCT...
ENST00000706901.1:c.896-51_896-48delinsCTGG ENSP00000516612.1:n.896-51_896-48delinsCT...
ENST00000706902.1:c.896-51_896-48delinsCTGG ENSP00000516613.1:n.896-51_896-48delinsCT...
ENST00000706903.1:c.896-51_896-48delinsCTGG ENSP00000516614.1:n.896-51_896-48delinsCT...
ENST00000706904.1:c.896-51_896-48delinsCTGG ENSP00000516615.1:n.896-51_896-48delinsCT...
ENST00000706905.1:c.896-51_896-48delinsCTGG ENSP00000516616.1:n.896-51_896-48delinsCT...
ENST00000376809.10:c.896-51_896-48delinsCTGG MANE Select ENSP00000366005.5:n.896-51_896-48delinsCT...
ENST00000638375.1:c.895+52_895+55delinsCTGG ENSP00000492789.1:n.895+52_895+55delinsCT...
ENST00000376802.2:c.895+52_895+55delinsCTGG ENSP00000365998.2:n.895+52_895+55delinsCT...
ENST00000376806.9:c.896-51_896-48delinsCTGG ENSP00000366002.5:n.896-51_896-48delinsCT...
ENST00000376809.9:c.896-51_896-48delinsCTGG ENSP00000366005.5:n.896-51_896-48delinsCT...
ENST00000396634.5:c.896-51_896-48delinsCTGG ENSP00000379873.1:n.896-51_896-48delinsCT...
ENST00000461903.1:n.1137-51_1137-48delinsCTGG
ENST00000479320.5:n.1137-51_1137-48delinsCTGG
ENST00000495183.5:n.1139-51_1139-48delinsCTGG
ENST00000496081.5:n.713-51_713-48delinsCTGG
NM_002116.7:c.896-51_896-48delinsCTGG NP_002107.3:n.896-51_896-48delinsCTGG
NM_002116.8:c.896-51_896-48delinsCTGG MANE Select NP_002107.3:n.896-51_896-48delinsCTGG