Canonical Allele Identifier: CA1619079077

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270118_31270125delinsCCCCCAAG , CM000668.2:g.31270118_31270125delinsCCCCCAAG	GRCh38
NC_000006.11:g.31237895_31237902delinsCCCCCAAG , CM000668.1:g.31237895_31237902delinsCCCCCAAG	GRCh37
NC_000006.10:g.31345874_31345881delinsCCCCCAAG	NCBI36
NG_029422.2:g.7007_7014delinsCTTGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.896-40_896-33delinsCTTGGGGG MANE Select	ENSP00000365402.5:n.896-40_896-33delinsCTTGGGGG
ENST00000376228.9:c.896-40_896-33delinsCTTGGGGG	ENSP00000365402.5:n.896-40_896-33delinsCTTGGGGG
ENST00000376237.8:c.*483-40_*483-33delinsCTTGGGGG	ENSP00000365412.4:n.*483-40_*483-33delinsCTTGGGGG
ENST00000383329.7:c.896-40_896-33delinsCTTGGGGG	ENSP00000372819.3:n.896-40_896-33delinsCTTGGGGG
ENST00000470363.5:n.214-40_214-33delinsCTTGGGGG
ENST00000487245.5:n.1255-40_1255-33delinsCTTGGGGG
NM_002117.5:c.896-40_896-33delinsCTTGGGGG	NP_002108.4:n.896-40_896-33delinsCTTGGGGG
NM_002117.6:c.896-40_896-33delinsCTTGGGGG MANE Select	NP_002108.4:n.896-40_896-33delinsCTTGGGGG