Canonical Allele Identifier: CA2711335548

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113910933

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271264_31271277del , CM000668.2:g.31271264_31271277del	GRCh38
NC_000006.11:g.31239041_31239054del , CM000668.1:g.31239041_31239054del	GRCh37
NC_000006.10:g.31347020_31347033del	NCBI36
NG_029422.2:g.5856_5869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.416_429del MANE Select	ENSP00000365402.5:p.Gln139ArgfsTer?
ENST00000376228.9:c.416_429del	ENSP00000365402.5:p.Gln139ArgfsTer?
ENST00000376237.8:c.*3_*16del	ENSP00000365412.4:n.*3_*16del
ENST00000383329.7:c.416_429del	ENSP00000372819.3:p.Gln139ArgfsTer?
ENST00000415537.1:c.414_427del
ENST00000484378.1:n.685_698del
ENST00000487245.5:n.775_788del
ENST00000495835.1:n.605_618del
NM_002117.5:c.416_429del	NP_002108.4:p.Gln139ArgfsTer?
NM_002117.6:c.416_429del MANE Select	NP_002108.4:p.Gln139ArgfsTer?