Canonical Allele Identifier: CA2770491530

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269396_31269397insAAAA , CM000668.2:g.31269396_31269397insAAAA	GRCh38
NC_000006.11:g.31237173_31237174insAAAA , CM000668.1:g.31237173_31237174insAAAA	GRCh37
NC_000006.10:g.31345152_31345153insAAAA	NCBI36
NG_029422.2:g.7737_7738insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-10_1049-9insTTTT MANE Select	ENSP00000365402.5:n.1049-10_1049-9insTTTT
ENST00000376228.9:c.1049-10_1049-9insTTTT	ENSP00000365402.5:n.1049-10_1049-9insTTTT
ENST00000376237.8:c.*636-10_*636-9insTTTT	ENSP00000365412.4:n.*636-10_*636-9insTTTT
ENST00000383329.7:c.1067-10_1067-9insTTTT	ENSP00000372819.3:n.1067-10_1067-9insTTTT
ENST00000466892.5:n.272_273insTTTT
ENST00000470363.5:n.807-10_807-9insTTTT
ENST00000487245.5:n.1408-10_1408-9insTTTT
NM_002117.5:c.1049-10_1049-9insTTTT	NP_002108.4:n.1049-10_1049-9insTTTT
NM_002117.6:c.1049-10_1049-9insTTTT MANE Select	NP_002108.4:n.1049-10_1049-9insTTTT