Canonical Allele Identifier: CA1435773370
Gene: WFS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302944G= , CM000666.2:g.6302944G= GRCh38
NC_000004.11:g.6304671G= , CM000666.1:g.6304671G= GRCh37
NC_000004.10:g.6355572G= NCBI36
NG_011700.1:g.38095G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*476G= ENSP00000507852.1:n.*476G=
ENST00000683395.1:c.3126G=
ENST00000684087.1:c.*476G= ENSP00000506978.1:n.*476G=
ENST00000673991.1:c.*476G= ENSP00000501033.1:n.*476G=
ENST00000226760.5:c.*476G= MANE Select ENSP00000226760.1:n.*476G=
ENST00000507765.1:n.3334G=
NM_001145853.1:c.*476G= NP_001139325.1:n.*476G=
NM_006005.3:c.*476G= MANE Select NP_005996.2:n.*476G=
XM_017008586.1:c.*476G= XP_016864075.1:n.*476G=
XR_001741566.2:n.2001C=
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