Canonical Allele Identifier: CA1619078330

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761142229
• gnomAD v4: 6-31269727-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269728_31269729del , CM000668.2:g.31269728_31269729del	GRCh38
NC_000006.11:g.31237505_31237506del , CM000668.1:g.31237505_31237506del	GRCh37
NC_000006.10:g.31345484_31345485del	NCBI36
NG_029422.2:g.7403_7404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1016-204_1016-203del MANE Select	ENSP00000365402.5:n.1016-204_1016-203del
ENST00000376228.9:c.1016-204_1016-203del	ENSP00000365402.5:n.1016-204_1016-203del
ENST00000376237.8:c.*603-204_*603-203del	ENSP00000365412.4:n.*603-204_*603-203del
ENST00000383329.7:c.1016-186_1016-185del	ENSP00000372819.3:n.1016-186_1016-185del
ENST00000470363.5:n.570_571del
ENST00000487245.5:n.1375-204_1375-203del
NM_002117.5:c.1016-204_1016-203del	NP_002108.4:n.1016-204_1016-203del
NM_002117.6:c.1016-204_1016-203del MANE Select	NP_002108.4:n.1016-204_1016-203del