Canonical Allele Identifier: CA1619079055

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270107_31270108delinsAG , CM000668.2:g.31270107_31270108delinsAG	GRCh38
NC_000006.11:g.31237884_31237885delinsAG , CM000668.1:g.31237884_31237885delinsAG	GRCh37
NC_000006.10:g.31345863_31345864delinsAG	NCBI36
NG_029422.2:g.7024_7025delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.896-23_896-22delinsCT MANE Select	ENSP00000365402.5:n.896-23_896-22delinsCT
ENST00000376228.9:c.896-23_896-22delinsCT	ENSP00000365402.5:n.896-23_896-22delinsCT
ENST00000376237.8:c.*483-23_*483-22delinsCT	ENSP00000365412.4:n.*483-23_*483-22delinsCT
ENST00000383329.7:c.896-23_896-22delinsCT	ENSP00000372819.3:n.896-23_896-22delinsCT
ENST00000470363.5:n.214-23_214-22delinsCT
ENST00000487245.5:n.1255-23_1255-22delinsCT
NM_002117.5:c.896-23_896-22delinsCT	NP_002108.4:n.896-23_896-22delinsCT
NM_002117.6:c.896-23_896-22delinsCT MANE Select	NP_002108.4:n.896-23_896-22delinsCT