Canonical Allele Identifier: CA1435769004

Gene: WFS1

Linked Data

• dbSNP Id: rs1730479451

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6292016_6292031dup , CM000666.2:g.6292016_6292031dup	GRCh38
NC_000004.11:g.6293743_6293758dup , CM000666.1:g.6293743_6293758dup	GRCh37
NC_000004.10:g.6344644_6344659dup	NCBI36
NG_011700.1:g.27167_27182dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.712+19_712+34dup	ENSP00000507852.1:n.712+19_712+34dup
ENST00000683395.1:c.689+19_689+34dup
ENST00000684087.1:c.712+19_712+34dup	ENSP00000506978.1:n.712+19_712+34dup
ENST00000506362.2:c.463+19_463+34dup	ENSP00000424103.2:n.463+19_463+34dup
ENST00000673642.1:c.511+19_511+34dup	ENSP00000501242.1:n.511+19_511+34dup
ENST00000673991.1:c.712+19_712+34dup	ENSP00000501033.1:n.712+19_712+34dup
ENST00000226760.5:c.712+19_712+34dup MANE Select	ENSP00000226760.1:n.712+19_712+34dup
ENST00000503569.5:c.712+19_712+34dup	ENSP00000423337.1:n.712+19_712+34dup
ENST00000506362.1:c.309+19_309+34dup
ENST00000507765.1:n.897+19_897+34dup
NM_001145853.1:c.712+19_712+34dup	NP_001139325.1:n.712+19_712+34dup
NM_006005.3:c.712+19_712+34dup MANE Select	NP_005996.2:n.712+19_712+34dup
XM_017008586.1:c.721+19_721+34dup	XP_016864075.1:n.721+19_721+34dup