Canonical Allele Identifier: CA356176059

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303101A>T (hg19) ; chr4:g.6301374A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301374A>T , CM000666.2:g.6301374A>T	GRCh38
NC_000004.11:g.6303101A>T , CM000666.1:g.6303101A>T	GRCh37
NC_000004.10:g.6354002A>T	NCBI36
NG_011700.1:g.36525A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1615A>T	ENSP00000507852.1:p.Thr539Ser
ENST00000683395.1:c.1556A>T
ENST00000684087.1:c.1579A>T	ENSP00000506978.1:p.Thr527Ser
ENST00000506362.2:c.1330A>T	ENSP00000424103.2:p.Thr444Ser
ENST00000673642.1:c.1238A>T	ENSP00000501242.1:p.His413Leu
ENST00000673991.1:c.1615A>T	ENSP00000501033.1:p.Thr539Ser
ENST00000226760.5:c.1579A>T MANE Select	ENSP00000226760.1:p.Thr527Ser
ENST00000503569.5:c.1579A>T	ENSP00000423337.1:p.Thr527Ser
ENST00000507765.1:n.1764A>T
NM_001145853.1:c.1579A>T	NP_001139325.1:p.Thr527Ser
NM_006005.3:c.1579A>T MANE Select	NP_005996.2:p.Thr527Ser
XM_017008586.1:c.1588A>T	XP_016864075.1:p.Thr530Ser