Canonical Allele Identifier: CA1619080648
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271490_31271495delinsGCAGAT , CM000668.2:g.31271490_31271495delinsGCAGAT GRCh38
NC_000006.11:g.31239267_31239272delinsGCAGAT , CM000668.1:g.31239267_31239272delinsGCAGAT GRCh37
NC_000006.10:g.31347246_31347251delinsGCAGAT NCBI36
NG_029422.2:g.5637_5642delinsATCTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+104_343+109delinsATCTGC MANE Select ENSP00000365402.5:n.343+104_343+109delins...
ENST00000376228.9:c.343+104_343+109delinsATCTGC ENSP00000365402.5:n.343+104_343+109delins...
ENST00000376237.8:c.343+104_343+109delinsATCTGC ENSP00000365412.4:n.343+104_343+109delins...
ENST00000383329.7:c.343+104_343+109delinsATCTGC ENSP00000372819.3:n.343+104_343+109delins...
ENST00000415537.1:c.341+104_341+109delinsATCTGC
ENST00000484378.1:n.466_471delinsATCTGC
ENST00000487245.5:n.556_561delinsATCTGC
ENST00000495835.1:n.532+104_532+109delinsATCTGC
NM_002117.5:c.343+104_343+109delinsATCTGC NP_002108.4:n.343+104_343+109delinsATCTGC...
NM_002117.6:c.343+104_343+109delinsATCTGC MANE Select NP_002108.4:n.343+104_343+109delinsATCTGC...