Canonical Allele Identifier: CA2677951692

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271601-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271601_31271602insTG , CM000668.2:g.31271601_31271602insTG	GRCh38
NC_000006.11:g.31239378_31239379insTG , CM000668.1:g.31239378_31239379insTG	GRCh37
NC_000006.10:g.31347357_31347358insTG	NCBI36
NG_029422.2:g.5530_5531insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.340_341insCA MANE Select	ENSP00000365402.5:p.Asp114AlafsTer?
ENST00000376228.9:c.340_341insCA	ENSP00000365402.5:p.Asp114AlafsTer?
ENST00000376237.8:c.340_341insCA	ENSP00000365412.4:p.Asp114AlafsTer?
ENST00000383329.7:c.340_341insCA	ENSP00000372819.3:p.Asp114AlafsTer?
ENST00000415537.1:c.338_339insCA
ENST00000484378.1:n.359_360insCA
ENST00000487245.5:n.449_450insCA
ENST00000495835.1:n.529_530insCA
NM_002117.5:c.340_341insCA	NP_002108.4:p.Asp114AlafsTer?
NM_002117.6:c.340_341insCA MANE Select	NP_002108.4:p.Asp114AlafsTer?