Canonical Allele Identifier: CA2677950678

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270356-TGGGTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270357_31270361del , CM000668.2:g.31270357_31270361del	GRCh38
NC_000006.11:g.31238134_31238138del , CM000668.1:g.31238134_31238138del	GRCh37
NC_000006.10:g.31346113_31346117del	NCBI36
NG_029422.2:g.6771_6775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.744_748del MANE Select	ENSP00000365402.5:p.Thr249GlyfsTer?
ENST00000376228.9:c.744_748del	ENSP00000365402.5:p.Thr249GlyfsTer?
ENST00000376237.8:c.*331_*335del	ENSP00000365412.4:n.*331_*335del
ENST00000383329.7:c.744_748del	ENSP00000372819.3:p.Thr249GlyfsTer?
ENST00000415537.1:c.665-30_665-26del
ENST00000470363.5:n.62_66del
ENST00000487245.5:n.1103_1107del
ENST00000495835.1:n.933_937del
NM_002117.5:c.744_748del	NP_002108.4:p.Thr249GlyfsTer?
NM_002117.6:c.744_748del MANE Select	NP_002108.4:p.Thr249GlyfsTer?