Canonical Allele Identifier: CA356172025

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291292-A-T
• MyVariant Identifiers: chr4:g.6293019A>T (hg19) ; chr4:g.6291292A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291292A>T , CM000666.2:g.6291292A>T	GRCh38
NC_000004.11:g.6293019A>T , CM000666.1:g.6293019A>T	GRCh37
NC_000004.10:g.6343920A>T	NCBI36
NG_011700.1:g.26443A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.556A>T	ENSP00000507852.1:p.Lys186Ter
ENST00000683395.1:c.546A>T
ENST00000684087.1:c.556A>T	ENSP00000506978.1:p.Lys186Ter
ENST00000684700.1:c.556A>T	ENSP00000507806.1:p.Lys186Ter
ENST00000506362.2:c.307A>T	ENSP00000424103.2:p.Lys103Ter
ENST00000673642.1:c.355A>T	ENSP00000501242.1:p.Lys119Ter
ENST00000673991.1:c.556A>T	ENSP00000501033.1:p.Lys186Ter
ENST00000674051.1:c.430A>T	ENSP00000501083.1:p.Lys144Ter
ENST00000226760.5:c.556A>T MANE Select	ENSP00000226760.1:p.Lys186Ter
ENST00000503569.5:c.556A>T	ENSP00000423337.1:p.Lys186Ter
ENST00000506362.1:c.153A>T
ENST00000507765.1:n.741A>T
NM_001145853.1:c.556A>T	NP_001139325.1:p.Lys186Ter
NM_006005.3:c.556A>T MANE Select	NP_005996.2:p.Lys186Ter
XM_017008586.1:c.565A>T	XP_016864075.1:p.Lys189Ter