Canonical Allele Identifier: CA2669826017

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291431-CCTTCCCATAGGGGCTGGGACCTTCCCTCAGGGGCTGGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291439_6291477del , CM000666.2:g.6291439_6291477del	GRCh38
NC_000004.11:g.6293166_6293204del , CM000666.1:g.6293166_6293204del	GRCh37
NC_000004.10:g.6344067_6344105del	NCBI36
NG_011700.1:g.26590_26628del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.631+72_631+110del	ENSP00000507852.1:n.631+72_631+110del
ENST00000683395.1:c.608+85_608+123del
ENST00000684087.1:c.631+72_631+110del	ENSP00000506978.1:n.631+72_631+110del
ENST00000684700.1:c.703_*36del	ENSP00000507806.1:n.[c.703_*36del;Ter235GlnextTer8]
ENST00000506362.2:c.382+72_382+110del	ENSP00000424103.2:n.382+72_382+110del
ENST00000673642.1:c.430+72_430+110del	ENSP00000501242.1:n.430+72_430+110del
ENST00000673991.1:c.631+72_631+110del	ENSP00000501033.1:n.631+72_631+110del
ENST00000226760.5:c.631+72_631+110del MANE Select	ENSP00000226760.1:n.631+72_631+110del
ENST00000503569.5:c.631+72_631+110del	ENSP00000423337.1:n.631+72_631+110del
ENST00000506362.1:c.228+72_228+110del
ENST00000507765.1:n.816+72_816+110del
NM_001145853.1:c.631+72_631+110del	NP_001139325.1:n.631+72_631+110del
NM_006005.3:c.631+72_631+110del MANE Select	NP_005996.2:n.631+72_631+110del
XM_017008586.1:c.640+72_640+110del	XP_016864075.1:n.640+72_640+110del