Canonical Allele Identifier: CA1435773318
Gene: WFS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302892T= , CM000666.2:g.6302892T= GRCh38
NC_000004.11:g.6304619T= , CM000666.1:g.6304619T= GRCh37
NC_000004.10:g.6355520T= NCBI36
NG_011700.1:g.38043T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*424T= ENSP00000507852.1:n.*424T=
ENST00000683395.1:c.3074T=
ENST00000684087.1:c.*424T= ENSP00000506978.1:n.*424T=
ENST00000673991.1:c.*424T= ENSP00000501033.1:n.*424T=
ENST00000226760.5:c.*424T= MANE Select ENSP00000226760.1:n.*424T=
ENST00000507765.1:n.3282T=
NM_001145853.1:c.*424T= NP_001139325.1:n.*424T=
NM_006005.3:c.*424T= MANE Select NP_005996.2:n.*424T=
XM_017008586.1:c.*424T= XP_016864075.1:n.*424T=
XR_001741566.2:n.2053A=
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