Canonical Allele Identifier: CA2677949093

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31268902-TGCACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268903_31268907del , CM000668.2:g.31268903_31268907del	GRCh38
NC_000006.11:g.31236680_31236684del , CM000668.1:g.31236680_31236684del	GRCh37
NC_000006.10:g.31344659_31344663del	NCBI36
NG_029422.2:g.8225_8229del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*262_*266del MANE Select	ENSP00000365402.5:n.*262_*266del
ENST00000376228.9:c.*262_*266del	ENSP00000365402.5:n.*262_*266del
ENST00000376237.8:c.*950_*954del	ENSP00000365412.4:n.*950_*954del
ENST00000383329.7:c.*262_*266del	ENSP00000372819.3:n.*262_*266del
ENST00000466892.5:n.596_600del
ENST00000470363.5:n.1121_1125del
ENST00000487245.5:n.1722_1726del
NM_002117.5:c.*262_*266del	NP_002108.4:n.*262_*266del
NM_002117.6:c.*262_*266del MANE Select	NP_002108.4:n.*262_*266del