Canonical Allele Identifier: CA1619080235

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761273948

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271005_31271009del , CM000668.2:g.31271005_31271009del	GRCh38
NC_000006.11:g.31238782_31238786del , CM000668.1:g.31238782_31238786del	GRCh37
NC_000006.10:g.31346761_31346765del	NCBI36
NG_029422.2:g.6128_6132del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.619+69_619+73del MANE Select	ENSP00000365402.5:n.619+69_619+73del
ENST00000376228.9:c.619+69_619+73del	ENSP00000365402.5:n.619+69_619+73del
ENST00000376237.8:c.*206+69_*206+73del	ENSP00000365412.4:n.*206+69_*206+73del
ENST00000383329.7:c.619+69_619+73del	ENSP00000372819.3:n.619+69_619+73del
ENST00000415537.1:c.617+69_617+73del
ENST00000487245.5:n.978+69_978+73del
ENST00000495835.1:n.808+69_808+73del
NM_002117.5:c.619+69_619+73del	NP_002108.4:n.619+69_619+73del
NM_002117.6:c.619+69_619+73del MANE Select	NP_002108.4:n.619+69_619+73del