Canonical Allele Identifier: CA2677950687
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270377del , CM000668.2:g.31270377del GRCh38
NC_000006.11:g.31238154del , CM000668.1:g.31238154del GRCh37
NC_000006.10:g.31346133del NCBI36
NG_029422.2:g.6757del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.730del MANE Select ENSP00000365402.5:p.Asp244MetfsTer?
ENST00000376228.9:c.730del ENSP00000365402.5:p.Asp244MetfsTer?
ENST00000376237.8:c.*317del ENSP00000365412.4:n.*317del
ENST00000383329.7:c.730del ENSP00000372819.3:p.Asp244MetfsTer?
ENST00000415537.1:c.665-44del
ENST00000470363.5:n.48del
ENST00000487245.5:n.1089del
ENST00000495835.1:n.919del
NM_002117.5:c.730del NP_002108.4:p.Asp244MetfsTer?
NM_002117.6:c.730del MANE Select NP_002108.4:p.Asp244MetfsTer?