Canonical Allele Identifier: CA2677951357
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271336_31271337insTGATGTGAGACCCT , CM000668.2:g.31271336_31271337insTGATGTGAGACCCT GRCh38
NC_000006.11:g.31239113_31239114insTGATGTGAGACCCT , CM000668.1:g.31239113_31239114insTGATGTGAGACCCT GRCh37
NC_000006.10:g.31347092_31347093insTGATGTGAGACCCT NCBI36
NG_029422.2:g.5795_5796insAGGGTCTCACATCA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.355_356insAGGGTCTCACATCA MANE Select ENSP00000365402.5:p.Leu119GlnfsTer?
ENST00000376228.9:c.355_356insAGGGTCTCACATCA ENSP00000365402.5:p.Leu119GlnfsTer?
ENST00000376237.8:c.344-6_344-5insAGGGTCTCACATCA ENSP00000365412.4:n.344-6_344-5insAGGGTCT...
ENST00000383329.7:c.355_356insAGGGTCTCACATCA ENSP00000372819.3:p.Leu119GlnfsTer?
ENST00000415537.1:c.353_354insAGGGTCTCACATCA
ENST00000484378.1:n.624_625insAGGGTCTCACATCA
ENST00000487245.5:n.714_715insAGGGTCTCACATCA
ENST00000495835.1:n.544_545insAGGGTCTCACATCA
NM_002117.5:c.355_356insAGGGTCTCACATCA NP_002108.4:p.Leu119GlnfsTer?
NM_002117.6:c.355_356insAGGGTCTCACATCA MANE Select NP_002108.4:p.Leu119GlnfsTer?