Canonical Allele Identifier: CA1619079078

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270118_31270137delinsCCCCCAAGCCTCAGCCCTGA , CM000668.2:g.31270118_31270137delinsCCCCCAAGCCTCAGCCCTGA	GRCh38
NC_000006.11:g.31237895_31237914delinsCCCCCAAGCCTCAGCCCTGA , CM000668.1:g.31237895_31237914delinsCCCCCAAGCCTCAGCCCTGA	GRCh37
NC_000006.10:g.31345874_31345893delinsCCCCCAAGCCTCAGCCCTGA	NCBI36
NG_029422.2:g.6995_7014delinsTCAGGGCTGAGGCTTGGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.896-52_896-33delinsTCAGGGCTGAGGCTTGGGGG MANE Select	ENSP00000365402.5:n.896-52_896-33delinsTC...
ENST00000376228.9:c.896-52_896-33delinsTCAGGGCTGAGGCTTGGGGG	ENSP00000365402.5:n.896-52_896-33delinsTC...
ENST00000376237.8:c.*483-52_*483-33delinsTCAGGGCTGAGGCTTGGGGG	ENSP00000365412.4:n.*483-52_*483-33delins...
ENST00000383329.7:c.896-52_896-33delinsTCAGGGCTGAGGCTTGGGGG	ENSP00000372819.3:n.896-52_896-33delinsTC...
ENST00000470363.5:n.214-52_214-33delinsTCAGGGCTGAGGCTTGGGGG
ENST00000487245.5:n.1255-52_1255-33delinsTCAGGGCTGAGGCTTGGGGG
NM_002117.5:c.896-52_896-33delinsTCAGGGCTGAGGCTTGGGGG	NP_002108.4:n.896-52_896-33delinsTCAGGGCT...
NM_002117.6:c.896-52_896-33delinsTCAGGGCTGAGGCTTGGGGG MANE Select	NP_002108.4:n.896-52_896-33delinsTCAGGGCT...