Canonical Allele Identifier: CA1435768709
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291471C= , CM000666.2:g.6291471C= GRCh38
NC_000004.11:g.6293198C= , CM000666.1:g.6293198C= GRCh37
NC_000004.10:g.6344099C= NCBI36
NG_011700.1:g.26622C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.631+104C= ENSP00000507852.1:n.631+104C=
ENST00000683395.1:c.608+117C=
ENST00000684087.1:c.631+104C= ENSP00000506978.1:n.631+104C=
ENST00000684700.1:c.*30C= ENSP00000507806.1:n.*30C=
ENST00000506362.2:c.382+104C= ENSP00000424103.2:n.382+104C=
ENST00000673642.1:c.430+104C= ENSP00000501242.1:n.430+104C=
ENST00000673991.1:c.631+104C= ENSP00000501033.1:n.631+104C=
ENST00000226760.5:c.631+104C= MANE Select ENSP00000226760.1:n.631+104C=
ENST00000503569.5:c.631+104C= ENSP00000423337.1:n.631+104C=
ENST00000506362.1:c.228+104C=
ENST00000507765.1:n.816+104C=
NM_001145853.1:c.631+104C= NP_001139325.1:n.631+104C=
NM_006005.3:c.631+104C= MANE Select NP_005996.2:n.631+104C=
XM_017008586.1:c.640+104C= XP_016864075.1:n.640+104C=