Canonical Allele Identifier: CA1435773030
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs954434481
gnomAD v4: 4-6302622-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302622C>A , CM000666.2:g.6302622C>A GRCh38
NC_000004.11:g.6304349C>A , CM000666.1:g.6304349C>A GRCh37
NC_000004.10:g.6355250C>A NCBI36
NG_011700.1:g.37773C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.*154C>A ENSP00000507852.1:n.*154C>A
ENST00000683395.1:c.2804C>A
ENST00000684087.1:c.*154C>A ENSP00000506978.1:n.*154C>A
ENST00000506362.2:c.*154C>A ENSP00000424103.2:n.*154C>A
ENST00000673991.1:c.*154C>A ENSP00000501033.1:n.*154C>A
ENST00000226760.5:c.*154C>A MANE Select ENSP00000226760.1:n.*154C>A
ENST00000503569.5:c.*154C>A ENSP00000423337.1:n.*154C>A
ENST00000507765.1:n.3012C>A
NM_001145853.1:c.*154C>A NP_001139325.1:n.*154C>A
NM_006005.3:c.*154C>A MANE Select NP_005996.2:n.*154C>A
XM_017008586.1:c.*154C>A XP_016864075.1:n.*154C>A
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