Canonical Allele Identifier: CA2677951225

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271102-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271103_31271104del , CM000668.2:g.31271103_31271104del	GRCh38
NC_000006.11:g.31238880_31238881del , CM000668.1:g.31238880_31238881del	GRCh37
NC_000006.10:g.31346859_31346860del	NCBI36
NG_029422.2:g.6028_6029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.588_589del MANE Select	ENSP00000365402.5:p.Asn198ArgfsTer22
ENST00000376228.9:c.588_589del	ENSP00000365402.5:p.Asn198ArgfsTer22
ENST00000376237.8:c.*175_*176del	ENSP00000365412.4:n.*175_*176del
ENST00000383329.7:c.588_589del	ENSP00000372819.3:p.Asn198ArgfsTer22
ENST00000415537.1:c.586_587del
ENST00000484378.1:n.857_858del
ENST00000487245.5:n.947_948del
ENST00000495835.1:n.777_778del
NM_002117.5:c.588_589del	NP_002108.4:p.Asn198ArgfsTer22
NM_002117.6:c.588_589del MANE Select	NP_002108.4:p.Asn198ArgfsTer22