Canonical Allele Identifier: CA2677950229
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269920del , CM000668.2:g.31269920del GRCh38
NC_000006.11:g.31237697del , CM000668.1:g.31237697del GRCh37
NC_000006.10:g.31345676del NCBI36
NG_029422.2:g.7214del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+48del MANE Select ENSP00000365402.5:n.1015+48del
ENST00000376228.9:c.1015+48del ENSP00000365402.5:n.1015+48del
ENST00000376237.8:c.*602+48del ENSP00000365412.4:n.*602+48del
ENST00000383329.7:c.1015+48del ENSP00000372819.3:n.1015+48del
ENST00000470363.5:n.381del
ENST00000487245.5:n.1374+48del
NM_002117.5:c.1015+48del NP_002108.4:n.1015+48del
NM_002117.6:c.1015+48del MANE Select NP_002108.4:n.1015+48del