Canonical Allele Identifier: CA1087449849

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113901694
• gnomAD v3: 6-31269323-T-TAGA
• gnomAD v4: 6-31269323-T-TAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269323_31269324insAGA , CM000668.2:g.31269323_31269324insAGA	GRCh38
NC_000006.11:g.31237100_31237101insAGA , CM000668.1:g.31237100_31237101insAGA	GRCh37
NC_000006.10:g.31345079_31345080insAGA	NCBI36
NG_029422.2:g.7808_7809insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1096+14_1096+15insTCT MANE Select	ENSP00000365402.5:n.1096+14_1096+15insTCT
ENST00000376228.9:c.1096+14_1096+15insTCT	ENSP00000365402.5:n.1096+14_1096+15insTCT
ENST00000376237.8:c.*683+14_*683+15insTCT	ENSP00000365412.4:n.*683+14_*683+15insTCT
ENST00000383329.7:c.1114+14_1114+15insTCT	ENSP00000372819.3:n.1114+14_1114+15insTCT
ENST00000466892.5:n.329+14_329+15insTCT
ENST00000470363.5:n.854+14_854+15insTCT
ENST00000487245.5:n.1455+14_1455+15insTCT
NM_002117.5:c.1096+14_1096+15insTCT	NP_002108.4:n.1096+14_1096+15insTCT
NM_002117.6:c.1096+14_1096+15insTCT MANE Select	NP_002108.4:n.1096+14_1096+15insTCT