Canonical Allele Identifier: CA2677951265
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271147_31271148del , CM000668.2:g.31271147_31271148del GRCh38
NC_000006.11:g.31238924_31238925del , CM000668.1:g.31238924_31238925del GRCh37
NC_000006.10:g.31346903_31346904del NCBI36
NG_029422.2:g.5984_5985del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.544_545del MANE Select ENSP00000365402.5:p.Ala182LeufsTer?
ENST00000376228.9:c.544_545del ENSP00000365402.5:p.Ala182LeufsTer?
ENST00000376237.8:c.*131_*132del ENSP00000365412.4:n.*131_*132del
ENST00000383329.7:c.544_545del ENSP00000372819.3:p.Ala182LeufsTer?
ENST00000415537.1:c.542_543del
ENST00000484378.1:n.813_814del
ENST00000487245.5:n.903_904del
ENST00000495835.1:n.733_734del
NM_002117.5:c.544_545del NP_002108.4:p.Ala182LeufsTer?
NM_002117.6:c.544_545del MANE Select NP_002108.4:p.Ala182LeufsTer?