Canonical Allele Identifier: CA2677950696
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270398-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270400del , CM000668.2:g.31270400del GRCh38
NC_000006.11:g.31238177del , CM000668.1:g.31238177del GRCh37
NC_000006.10:g.31346156del NCBI36
NG_029422.2:g.6733del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.706del MANE Select ENSP00000365402.5:p.Glu236ArgfsTer4
ENST00000376228.9:c.706del ENSP00000365402.5:p.Glu236ArgfsTer4
ENST00000376237.8:c.*293del ENSP00000365412.4:n.*293del
ENST00000383329.7:c.706del ENSP00000372819.3:p.Glu236ArgfsTer4
ENST00000415537.1:c.664+40del
ENST00000470363.5:n.24del
ENST00000487245.5:n.1065del
ENST00000495835.1:n.895del
NM_002117.5:c.706del NP_002108.4:p.Glu236ArgfsTer4
NM_002117.6:c.706del MANE Select NP_002108.4:p.Glu236ArgfsTer4
Search 100 bp 5'
Search 100 bp 3'