Canonical Allele Identifier: CA1619080091

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761251008

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270691del , CM000668.2:g.31270691del	GRCh38
NC_000006.11:g.31238468del , CM000668.1:g.31238468del	GRCh37
NC_000006.10:g.31346447del	NCBI36
NG_029422.2:g.6441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-206del MANE Select	ENSP00000365402.5:n.620-206del
ENST00000376228.9:c.620-206del	ENSP00000365402.5:n.620-206del
ENST00000376237.8:c.*207-206del	ENSP00000365412.4:n.*207-206del
ENST00000383329.7:c.620-206del	ENSP00000372819.3:n.620-206del
ENST00000415537.1:c.618-206del
ENST00000487245.5:n.979-206del
ENST00000495835.1:n.809-206del
NM_002117.5:c.620-206del	NP_002108.4:n.620-206del
NM_002117.6:c.620-206del MANE Select	NP_002108.4:n.620-206del