Canonical Allele Identifier: CA2677950017

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269728-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269729_31269730dup , CM000668.2:g.31269729_31269730dup	GRCh38
NC_000006.11:g.31237506_31237507dup , CM000668.1:g.31237506_31237507dup	GRCh37
NC_000006.10:g.31345485_31345486dup	NCBI36
NG_029422.2:g.7402_7403dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1016-205_1016-204dup MANE Select	ENSP00000365402.5:n.1016-205_1016-204dup
ENST00000376228.9:c.1016-205_1016-204dup	ENSP00000365402.5:n.1016-205_1016-204dup
ENST00000376237.8:c.*603-205_*603-204dup	ENSP00000365412.4:n.*603-205_*603-204dup
ENST00000383329.7:c.1016-187_1016-186dup	ENSP00000372819.3:n.1016-187_1016-186dup
ENST00000470363.5:n.569_570dup
ENST00000487245.5:n.1375-205_1375-204dup
NM_002117.5:c.1016-205_1016-204dup	NP_002108.4:n.1016-205_1016-204dup
NM_002117.6:c.1016-205_1016-204dup MANE Select	NP_002108.4:n.1016-205_1016-204dup