Canonical Allele Identifier: CA2669826099

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291506-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291506A>G , CM000666.2:g.6291506A>G	GRCh38
NC_000004.11:g.6293233A>G , CM000666.1:g.6293233A>G	GRCh37
NC_000004.10:g.6344134A>G	NCBI36
NG_011700.1:g.26657A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+139A>G	ENSP00000507852.1:n.631+139A>G
ENST00000683395.1:c.608+152A>G
ENST00000684087.1:c.631+139A>G	ENSP00000506978.1:n.631+139A>G
ENST00000684700.1:c.*65A>G	ENSP00000507806.1:n.*65A>G
ENST00000506362.2:c.382+139A>G	ENSP00000424103.2:n.382+139A>G
ENST00000673642.1:c.430+139A>G	ENSP00000501242.1:n.430+139A>G
ENST00000673991.1:c.631+139A>G	ENSP00000501033.1:n.631+139A>G
ENST00000226760.5:c.631+139A>G MANE Select	ENSP00000226760.1:n.631+139A>G
ENST00000503569.5:c.631+139A>G	ENSP00000423337.1:n.631+139A>G
ENST00000506362.1:c.228+139A>G
ENST00000507765.1:n.816+139A>G
NM_001145853.1:c.631+139A>G	NP_001139325.1:n.631+139A>G
NM_006005.3:c.631+139A>G MANE Select	NP_005996.2:n.631+139A>G
XM_017008586.1:c.640+139A>G	XP_016864075.1:n.640+139A>G