Canonical Allele Identifier: CA356172551

Gene: WFS1

Linked Data

• gnomAD v4: 4-6295120-C-A
• MyVariant Identifiers: chr4:g.6296847C>A (hg19) ; chr4:g.6295120C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6295120C>A , CM000666.2:g.6295120C>A	GRCh38
NC_000004.11:g.6296847C>A , CM000666.1:g.6296847C>A	GRCh37
NC_000004.10:g.6347748C>A	NCBI36
NG_011700.1:g.30271C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.828C>A	ENSP00000507852.1:p.Phe276Leu
ENST00000683395.1:c.769C>A
ENST00000684087.1:c.792C>A	ENSP00000506978.1:p.Phe264Leu
ENST00000506362.2:c.543C>A	ENSP00000424103.2:p.Phe181Leu
ENST00000673642.1:c.591C>A	ENSP00000501242.1:p.Phe197Leu
ENST00000673991.1:c.828C>A	ENSP00000501033.1:p.Phe276Leu
ENST00000226760.5:c.792C>A MANE Select	ENSP00000226760.1:p.Phe264Leu
ENST00000503569.5:c.792C>A	ENSP00000423337.1:p.Phe264Leu
ENST00000506362.1:c.425C>A
ENST00000507765.1:n.977C>A
ENST00000513395.1:n.350C>A
NM_001145853.1:c.792C>A	NP_001139325.1:p.Phe264Leu
NM_006005.3:c.792C>A MANE Select	NP_005996.2:p.Phe264Leu
XM_017008586.1:c.801C>A	XP_016864075.1:p.Phe267Leu