Canonical Allele Identifier: CA2677951319
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271259del , CM000668.2:g.31271259del GRCh38
NC_000006.11:g.31239036del , CM000668.1:g.31239036del GRCh37
NC_000006.10:g.31347015del NCBI36
NG_029422.2:g.5874del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.434del MANE Select ENSP00000365402.5:p.Lys145ArgfsTer6
ENST00000376228.9:c.434del ENSP00000365402.5:p.Lys145ArgfsTer6
ENST00000376237.8:c.*21del ENSP00000365412.4:n.*21del
ENST00000383329.7:c.434del ENSP00000372819.3:p.Lys145ArgfsTer6
ENST00000415537.1:c.432del
ENST00000484378.1:n.703del
ENST00000487245.5:n.793del
ENST00000495835.1:n.623del
NM_002117.5:c.434del NP_002108.4:p.Lys145ArgfsTer6
NM_002117.6:c.434del MANE Select NP_002108.4:p.Lys145ArgfsTer6