Canonical Allele Identifier: CA2677951594
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271527_31271536del , CM000668.2:g.31271527_31271536del GRCh38
NC_000006.11:g.31239304_31239313del , CM000668.1:g.31239304_31239313del GRCh37
NC_000006.10:g.31347283_31347292del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+66_343+75del MANE Select ENSP00000365402.5:n.343+66_343+75del
ENST00000376228.9:c.343+66_343+75del ENSP00000365402.5:n.343+66_343+75del
ENST00000376237.8:c.343+66_343+75del ENSP00000365412.4:n.343+66_343+75del
ENST00000383329.7:c.343+66_343+75del ENSP00000372819.3:n.343+66_343+75del
ENST00000415537.1:c.341+66_341+75del
ENST00000484378.1:n.428_437del
ENST00000487245.5:n.518_527del
ENST00000495835.1:n.532+66_532+75del
NM_002117.5:c.343+66_343+75del NP_002108.4:n.343+66_343+75del
NM_002117.6:c.343+66_343+75del MANE Select NP_002108.4:n.343+66_343+75del