Canonical Allele Identifier: CA1087425000
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270793_31270798del , CM000668.2:g.31270793_31270798del GRCh38
NC_000006.11:g.31238570_31238575del , CM000668.1:g.31238570_31238575del GRCh37
NC_000006.10:g.31346549_31346554del NCBI36
NG_029422.2:g.6334_6339del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+275_619+280del MANE Select ENSP00000365402.5:n.619+275_619+280del
ENST00000376228.9:c.619+275_619+280del ENSP00000365402.5:n.619+275_619+280del
ENST00000376237.8:c.*206+275_*206+280del ENSP00000365412.4:n.*206+275_*206+280del
ENST00000383329.7:c.619+275_619+280del ENSP00000372819.3:n.619+275_619+280del
ENST00000415537.1:c.617+275_617+280del
ENST00000487245.5:n.978+275_978+280del
ENST00000495835.1:n.808+275_808+280del
NM_002117.5:c.619+275_619+280del NP_002108.4:n.619+275_619+280del
NM_002117.6:c.619+275_619+280del MANE Select NP_002108.4:n.619+275_619+280del