Canonical Allele Identifier: CA2677951705
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271630_31271631insAGACA , CM000668.2:g.31271630_31271631insAGACA GRCh38
NC_000006.11:g.31239407_31239408insAGACA , CM000668.1:g.31239407_31239408insAGACA GRCh37
NC_000006.10:g.31347386_31347387insAGACA NCBI36
NG_029422.2:g.5501_5502insTGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.311_312insTGTCT MANE Select ENSP00000365402.5:p.Leu105ValfsTer?
ENST00000376228.9:c.311_312insTGTCT ENSP00000365402.5:p.Leu105ValfsTer?
ENST00000376237.8:c.311_312insTGTCT ENSP00000365412.4:p.Leu105ValfsTer?
ENST00000383329.7:c.311_312insTGTCT ENSP00000372819.3:p.Leu105ValfsTer?
ENST00000415537.1:c.309_310insTGTCT
ENST00000484378.1:n.330_331insTGTCT
ENST00000487245.5:n.420_421insTGTCT
ENST00000495835.1:n.500_501insTGTCT
NM_002117.5:c.311_312insTGTCT NP_002108.4:p.Leu105ValfsTer?
NM_002117.6:c.311_312insTGTCT MANE Select NP_002108.4:p.Leu105ValfsTer?