Canonical Allele Identifier: CA356173934

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6302464G>A (hg19) ; chr4:g.6300737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300737G>A , CM000666.2:g.6300737G>A	GRCh38
NC_000004.11:g.6302464G>A , CM000666.1:g.6302464G>A	GRCh37
NC_000004.10:g.6353365G>A	NCBI36
NG_011700.1:g.35888G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.978G>A	ENSP00000507852.1:p.Trp326Ter
ENST00000683395.1:c.919G>A
ENST00000684087.1:c.942G>A	ENSP00000506978.1:p.Trp314Ter
ENST00000506362.2:c.693G>A	ENSP00000424103.2:p.Trp231Ter
ENST00000673642.1:c.661-60G>A	ENSP00000501242.1:n.661-60G>A
ENST00000673991.1:c.978G>A	ENSP00000501033.1:p.Trp326Ter
ENST00000226760.5:c.942G>A MANE Select	ENSP00000226760.1:p.Trp314Ter
ENST00000503569.5:c.942G>A	ENSP00000423337.1:p.Trp314Ter
ENST00000506362.1:c.575G>A
ENST00000507765.1:n.1127G>A
ENST00000513395.1:n.500G>A
NM_001145853.1:c.942G>A	NP_001139325.1:p.Trp314Ter
NM_006005.3:c.942G>A MANE Select	NP_005996.2:p.Trp314Ter
XM_017008586.1:c.951G>A	XP_016864075.1:p.Trp317Ter