Canonical Allele Identifier: CA1087449768

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113901660
• gnomAD v3: 6-31269310-C-CCCCA
• gnomAD v4: 6-31269310-C-CCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269310_31269311insCCCA , CM000668.2:g.31269310_31269311insCCCA	GRCh38
NC_000006.11:g.31237087_31237088insCCCA , CM000668.1:g.31237087_31237088insCCCA	GRCh37
NC_000006.10:g.31345066_31345067insCCCA	NCBI36
NG_029422.2:g.7821_7822insTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1096+27_1096+28insTGGG MANE Select	ENSP00000365402.5:n.1096+27_1096+28insTGGG
ENST00000376228.9:c.1096+27_1096+28insTGGG	ENSP00000365402.5:n.1096+27_1096+28insTGGG
ENST00000376237.8:c.*683+27_*683+28insTGGG	ENSP00000365412.4:n.*683+27_*683+28insTGGG
ENST00000383329.7:c.1114+27_1114+28insTGGG	ENSP00000372819.3:n.1114+27_1114+28insTGGG
ENST00000466892.5:n.329+27_329+28insTGGG
ENST00000470363.5:n.854+27_854+28insTGGG
ENST00000487245.5:n.1455+27_1455+28insTGGG
NM_002117.5:c.1096+27_1096+28insTGGG	NP_002108.4:n.1096+27_1096+28insTGGG
NM_002117.6:c.1096+27_1096+28insTGGG MANE Select	NP_002108.4:n.1096+27_1096+28insTGGG