Canonical Allele Identifier: CA136860956

Gene: HLA-C

Linked Data

• dbSNP Id: rs796625701

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268869_31268870delinsTT , CM000668.2:g.31268869_31268870delinsTT	GRCh38
NC_000006.11:g.31236646_31236647delinsTT , CM000668.1:g.31236646_31236647delinsTT	GRCh37
NC_000006.10:g.31344625_31344626delinsTT	NCBI36
NG_029422.2:g.8262_8263delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*299_*300delinsAA MANE Select	ENSP00000365402.5:n.*299_*300delinsAA
ENST00000376228.9:c.*299_*300delinsAA	ENSP00000365402.5:n.*299_*300delinsAA
ENST00000376237.8:c.*987_*988delinsAA	ENSP00000365412.4:n.*987_*988delinsAA
ENST00000383329.7:c.*299_*300delinsAA	ENSP00000372819.3:n.*299_*300delinsAA
ENST00000466892.5:n.633_634delinsAA
ENST00000470363.5:n.1158_1159delinsAA
ENST00000487245.5:n.1759_1760delinsAA
NM_002117.5:c.*299_*300delinsAA	NP_002108.4:n.*299_*300delinsAA
NM_002117.6:c.*299_*300delinsAA MANE Select	NP_002108.4:n.*299_*300delinsAA