Canonical Allele Identifier: CA1619078308

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761141140

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269712_31269714del , CM000668.2:g.31269712_31269714del	GRCh38
NC_000006.11:g.31237489_31237491del , CM000668.1:g.31237489_31237491del	GRCh37
NC_000006.10:g.31345468_31345470del	NCBI36
NG_029422.2:g.7418_7420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1016-189_1016-187del MANE Select	ENSP00000365402.5:n.1016-189_1016-187del
ENST00000376228.9:c.1016-189_1016-187del	ENSP00000365402.5:n.1016-189_1016-187del
ENST00000376237.8:c.*603-189_*603-187del	ENSP00000365412.4:n.*603-189_*603-187del
ENST00000383329.7:c.1016-171_1016-169del	ENSP00000372819.3:n.1016-171_1016-169del
ENST00000470363.5:n.585_587del
ENST00000487245.5:n.1375-189_1375-187del
NM_002117.5:c.1016-189_1016-187del	NP_002108.4:n.1016-189_1016-187del
NM_002117.6:c.1016-189_1016-187del MANE Select	NP_002108.4:n.1016-189_1016-187del