Canonical Allele Identifier: CA566689030
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271336_31271337insTGATGTGAGACCCTGGCCCC , CM000668.2:g.31271336_31271337insTGATGTGAGACCCTGGCCCC GRCh38
NC_000006.11:g.31239113_31239114insTGATGTGAGACCCTGGCCCC , CM000668.1:g.31239113_31239114insTGATGTGAGACCCTGGCCCC GRCh37
NC_000006.10:g.31347092_31347093insTGATGTGAGACCCTGGCCCC NCBI36
NG_029422.2:g.5795_5796insGGGGCCAGGGTCTCACATCA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.355_356insGGGGCCAGGGTCTCACATCA MANE Select ENSP00000365402.5:p.Leu119ArgfsTer?
ENST00000376228.9:c.355_356insGGGGCCAGGGTCTCACATCA ENSP00000365402.5:p.Leu119ArgfsTer?
ENST00000376237.8:c.344-6_344-5insGGGGCCAGGGTCTCACATCA ENSP00000365412.4:n.344-6_344-5insGGGGCCA...
ENST00000383329.7:c.355_356insGGGGCCAGGGTCTCACATCA ENSP00000372819.3:p.Leu119ArgfsTer?
ENST00000415537.1:c.353_354insGGGGCCAGGGTCTCACATCA
ENST00000484378.1:n.624_625insGGGGCCAGGGTCTCACATCA
ENST00000487245.5:n.714_715insGGGGCCAGGGTCTCACATCA
ENST00000495835.1:n.544_545insGGGGCCAGGGTCTCACATCA
NM_002117.5:c.355_356insGGGGCCAGGGTCTCACATCA NP_002108.4:p.Leu119ArgfsTer?
NM_002117.6:c.355_356insGGGGCCAGGGTCTCACATCA MANE Select NP_002108.4:p.Leu119ArgfsTer?