Canonical Allele Identifier: CA1619077113

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268822_31268824delinsGCT , CM000668.2:g.31268822_31268824delinsGCT	GRCh38
NC_000006.11:g.31236599_31236601delinsGCT , CM000668.1:g.31236599_31236601delinsGCT	GRCh37
NC_000006.10:g.31344578_31344580delinsGCT	NCBI36
NG_029422.2:g.8308_8310delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*345_*347delinsAGC MANE Select	ENSP00000365402.5:n.*345_*347delinsAGC
ENST00000376228.9:c.*345_*347delinsAGC	ENSP00000365402.5:n.*345_*347delinsAGC
ENST00000376237.8:c.*1033_*1035delinsAGC	ENSP00000365412.4:n.*1033_*1035delinsAGC
ENST00000383329.7:c.*345_*347delinsAGC	ENSP00000372819.3:n.*345_*347delinsAGC
ENST00000466892.5:n.679_681delinsAGC
ENST00000470363.5:n.1204_1206delinsAGC
ENST00000487245.5:n.1805_1807delinsAGC
NM_002117.5:c.*345_*347delinsAGC	NP_002108.4:n.*345_*347delinsAGC
NM_002117.6:c.*345_*347delinsAGC MANE Select	NP_002108.4:n.*345_*347delinsAGC