Canonical Allele Identifier: CA1435773372
Gene: WFS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302946G= , CM000666.2:g.6302946G= GRCh38
NC_000004.11:g.6304673G= , CM000666.1:g.6304673G= GRCh37
NC_000004.10:g.6355574G= NCBI36
NG_011700.1:g.38097G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*478G= ENSP00000507852.1:n.*478G=
ENST00000683395.1:c.3128G=
ENST00000684087.1:c.*478G= ENSP00000506978.1:n.*478G=
ENST00000673991.1:c.*478G= ENSP00000501033.1:n.*478G=
ENST00000226760.5:c.*478G= MANE Select ENSP00000226760.1:n.*478G=
ENST00000507765.1:n.3336G=
NM_001145853.1:c.*478G= NP_001139325.1:n.*478G=
NM_006005.3:c.*478G= MANE Select NP_005996.2:n.*478G=
XM_017008586.1:c.*478G= XP_016864075.1:n.*478G=
XR_001741566.2:n.1999C=
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