Canonical Allele Identifier: CA1435768744
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291538A= , CM000666.2:g.6291538A= GRCh38
NC_000004.11:g.6293265A= , CM000666.1:g.6293265A= GRCh37
NC_000004.10:g.6344166A= NCBI36
NG_011700.1:g.26689A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.631+171A= ENSP00000507852.1:n.631+171A=
ENST00000683395.1:c.608+184A=
ENST00000684087.1:c.631+171A= ENSP00000506978.1:n.631+171A=
ENST00000684700.1:c.*97A= ENSP00000507806.1:n.*97A=
ENST00000506362.2:c.382+171A= ENSP00000424103.2:n.382+171A=
ENST00000673642.1:c.430+171A= ENSP00000501242.1:n.430+171A=
ENST00000673991.1:c.631+171A= ENSP00000501033.1:n.631+171A=
ENST00000226760.5:c.631+171A= MANE Select ENSP00000226760.1:n.631+171A=
ENST00000503569.5:c.631+171A= ENSP00000423337.1:n.631+171A=
ENST00000506362.1:c.228+171A=
ENST00000507765.1:n.816+171A=
NM_001145853.1:c.631+171A= NP_001139325.1:n.631+171A=
NM_006005.3:c.631+171A= MANE Select NP_005996.2:n.631+171A=
XM_017008586.1:c.640+171A= XP_016864075.1:n.640+171A=