Canonical Allele Identifier: CA2677950645

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270305-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270307_31270308del , CM000668.2:g.31270307_31270308del	GRCh38
NC_000006.11:g.31238084_31238085del , CM000668.1:g.31238084_31238085del	GRCh37
NC_000006.10:g.31346063_31346064del	NCBI36
NG_029422.2:g.6825_6826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.798_799del MANE Select	ENSP00000365402.5:p.Lys267ValfsTer?
ENST00000376228.9:c.798_799del	ENSP00000365402.5:p.Lys267ValfsTer?
ENST00000376237.8:c.*385_*386del	ENSP00000365412.4:n.*385_*386del
ENST00000383329.7:c.798_799del	ENSP00000372819.3:p.Lys267ValfsTer?
ENST00000415537.1:c.689_690del
ENST00000470363.5:n.116_117del
ENST00000487245.5:n.1157_1158del
ENST00000495835.1:n.987_988del
NM_002117.5:c.798_799del	NP_002108.4:p.Lys267ValfsTer?
NM_002117.6:c.798_799del MANE Select	NP_002108.4:p.Lys267ValfsTer?