Canonical Allele Identifier: CA2669843150

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300590-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300590G>T , CM000666.2:g.6300590G>T	GRCh38
NC_000004.11:g.6302317G>T , CM000666.1:g.6302317G>T	GRCh37
NC_000004.10:g.6353218G>T	NCBI36
NG_011700.1:g.35741G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-67G>T	ENSP00000507852.1:n.898-67G>T
ENST00000683395.1:c.839-67G>T
ENST00000684087.1:c.862-67G>T	ENSP00000506978.1:n.862-67G>T
ENST00000506362.2:c.613-67G>T	ENSP00000424103.2:n.613-67G>T
ENST00000673642.1:c.661-207G>T	ENSP00000501242.1:n.661-207G>T
ENST00000673991.1:c.898-67G>T	ENSP00000501033.1:n.898-67G>T
ENST00000226760.5:c.862-67G>T MANE Select	ENSP00000226760.1:n.862-67G>T
ENST00000503569.5:c.862-67G>T	ENSP00000423337.1:n.862-67G>T
ENST00000506362.1:c.495-67G>T
ENST00000507765.1:n.1047-67G>T
ENST00000513395.1:n.420-67G>T
NM_001145853.1:c.862-67G>T	NP_001139325.1:n.862-67G>T
NM_006005.3:c.862-67G>T MANE Select	NP_005996.2:n.862-67G>T
XM_017008586.1:c.871-67G>T	XP_016864075.1:n.871-67G>T