Canonical Allele Identifier: CA1435773956
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301546A= , CM000666.2:g.6301546A= GRCh38
NC_000004.11:g.6303273A= , CM000666.1:g.6303273A= GRCh37
NC_000004.10:g.6354174A= NCBI36
NG_011700.1:g.36697A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1787A= ENSP00000507852.1:p.Gln596=
ENST00000683395.1:c.1728A=
ENST00000684087.1:c.1751A= ENSP00000506978.1:p.Gln584=
ENST00000506362.2:c.1502A= ENSP00000424103.2:p.Gln501=
ENST00000673642.1:c.1410A= ENSP00000501242.1:n.1410A=
ENST00000673991.1:c.1787A= ENSP00000501033.1:p.Gln596=
ENST00000226760.5:c.1751A= MANE Select ENSP00000226760.1:p.Gln584=
ENST00000503569.5:c.1751A= ENSP00000423337.1:p.Gln584=
ENST00000507765.1:n.1936A=
NM_001145853.1:c.1751A= NP_001139325.1:p.Gln584=
NM_006005.3:c.1751A= MANE Select NP_005996.2:p.Gln584=
XM_017008586.1:c.1760A= XP_016864075.1:p.Gln587=