Canonical Allele Identifier: CA1619077150

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761085172

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268907_31268908insCAT , CM000668.2:g.31268907_31268908insCAT	GRCh38
NC_000006.11:g.31236684_31236685insCAT , CM000668.1:g.31236684_31236685insCAT	GRCh37
NC_000006.10:g.31344663_31344664insCAT	NCBI36
NG_029422.2:g.8224_8225insATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*261_*262insATG MANE Select	ENSP00000365402.5:n.*261_*262insATG
ENST00000376228.9:c.*261_*262insATG	ENSP00000365402.5:n.*261_*262insATG
ENST00000376237.8:c.*949_*950insATG	ENSP00000365412.4:n.*949_*950insATG
ENST00000383329.7:c.*261_*262insATG	ENSP00000372819.3:n.*261_*262insATG
ENST00000466892.5:n.595_596insATG
ENST00000470363.5:n.1120_1121insATG
ENST00000487245.5:n.1721_1722insATG
NM_002117.5:c.*261_*262insATG	NP_002108.4:n.*261_*262insATG
NM_002117.6:c.*261_*262insATG MANE Select	NP_002108.4:n.*261_*262insATG