Canonical Allele Identifier: CA2677951309
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271220-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271222del , CM000668.2:g.31271222del GRCh38
NC_000006.11:g.31238999del , CM000668.1:g.31238999del GRCh37
NC_000006.10:g.31346978del NCBI36
NG_029422.2:g.5911del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.471del MANE Select ENSP00000365402.5:p.Trp157Ter
ENST00000376228.9:c.471del ENSP00000365402.5:p.Trp157Ter
ENST00000376237.8:c.*58del ENSP00000365412.4:n.*58del
ENST00000383329.7:c.471del ENSP00000372819.3:p.Trp157Ter
ENST00000415537.1:c.469del
ENST00000484378.1:n.740del
ENST00000487245.5:n.830del
ENST00000495835.1:n.660del
NM_002117.5:c.471del NP_002108.4:p.Trp157Ter
NM_002117.6:c.471del MANE Select NP_002108.4:p.Trp157Ter
Search 100 bp 5'
Search 100 bp 3'