Canonical Allele Identifier: CA2677950474

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270113-CCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270114_31270116del , CM000668.2:g.31270114_31270116del	GRCh38
NC_000006.11:g.31237891_31237893del , CM000668.1:g.31237891_31237893del	GRCh37
NC_000006.10:g.31345870_31345872del	NCBI36
NG_029422.2:g.7016_7018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.896-31_896-29del MANE Select	ENSP00000365402.5:n.896-31_896-29del
ENST00000376228.9:c.896-31_896-29del	ENSP00000365402.5:n.896-31_896-29del
ENST00000376237.8:c.*483-31_*483-29del	ENSP00000365412.4:n.*483-31_*483-29del
ENST00000383329.7:c.896-31_896-29del	ENSP00000372819.3:n.896-31_896-29del
ENST00000470363.5:n.214-31_214-29del
ENST00000487245.5:n.1255-31_1255-29del
NM_002117.5:c.896-31_896-29del	NP_002108.4:n.896-31_896-29del
NM_002117.6:c.896-31_896-29del MANE Select	NP_002108.4:n.896-31_896-29del