Canonical Allele Identifier: CA2677951562

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271500-CTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271501_31271503del , CM000668.2:g.31271501_31271503del	GRCh38
NC_000006.11:g.31239278_31239280del , CM000668.1:g.31239278_31239280del	GRCh37
NC_000006.10:g.31347257_31347259del	NCBI36
NG_029422.2:g.5629_5631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+96_343+98del MANE Select	ENSP00000365402.5:n.343+96_343+98del
ENST00000376228.9:c.343+96_343+98del	ENSP00000365402.5:n.343+96_343+98del
ENST00000376237.8:c.343+96_343+98del	ENSP00000365412.4:n.343+96_343+98del
ENST00000383329.7:c.343+96_343+98del	ENSP00000372819.3:n.343+96_343+98del
ENST00000415537.1:c.341+96_341+98del
ENST00000484378.1:n.458_460del
ENST00000487245.5:n.548_550del
ENST00000495835.1:n.532+96_532+98del
NM_002117.5:c.343+96_343+98del	NP_002108.4:n.343+96_343+98del
NM_002117.6:c.343+96_343+98del MANE Select	NP_002108.4:n.343+96_343+98del