Canonical Allele Identifier: CA2677951237
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271119-CCA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271121_31271122del , CM000668.2:g.31271121_31271122del GRCh38
NC_000006.11:g.31238898_31238899del , CM000668.1:g.31238898_31238899del GRCh37
NC_000006.10:g.31346877_31346878del NCBI36
NG_029422.2:g.6011_6012del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.571_572del MANE Select ENSP00000365402.5:p.Trp191AlafsTer29
ENST00000376228.9:c.571_572del ENSP00000365402.5:p.Trp191AlafsTer29
ENST00000376237.8:c.*158_*159del ENSP00000365412.4:n.*158_*159del
ENST00000383329.7:c.571_572del ENSP00000372819.3:p.Trp191AlafsTer29
ENST00000415537.1:c.569_570del
ENST00000484378.1:n.840_841del
ENST00000487245.5:n.930_931del
ENST00000495835.1:n.760_761del
NM_002117.5:c.571_572del NP_002108.4:p.Trp191AlafsTer29
NM_002117.6:c.571_572del MANE Select NP_002108.4:p.Trp191AlafsTer29
Search 100 bp 5'
Search 100 bp 3'