Canonical Allele Identifier: CA356173936

Gene: WFS1

Linked Data

• dbSNP Id: rs752306040
• gnomAD v2: 4-6302465-C-G
• gnomAD v3: 4-6300738-C-G
• gnomAD v4: 4-6300738-C-G
• MyVariant Identifiers: chr4:g.6302465C>G (hg19) ; chr4:g.6300738C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300738C>G , CM000666.2:g.6300738C>G	GRCh38
NC_000004.11:g.6302465C>G , CM000666.1:g.6302465C>G	GRCh37
NC_000004.10:g.6353366C>G	NCBI36
NG_011700.1:g.35889C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.979C>G	ENSP00000507852.1:p.Leu327Val
ENST00000683395.1:c.920C>G
ENST00000684087.1:c.943C>G	ENSP00000506978.1:p.Leu315Val
ENST00000506362.2:c.694C>G	ENSP00000424103.2:p.Leu232Val
ENST00000673642.1:c.661-59C>G	ENSP00000501242.1:n.661-59C>G
ENST00000673991.1:c.979C>G	ENSP00000501033.1:p.Leu327Val
ENST00000226760.5:c.943C>G MANE Select	ENSP00000226760.1:p.Leu315Val
ENST00000503569.5:c.943C>G	ENSP00000423337.1:p.Leu315Val
ENST00000506362.1:c.576C>G
ENST00000507765.1:n.1128C>G
ENST00000513395.1:n.501C>G
NM_001145853.1:c.943C>G	NP_001139325.1:p.Leu315Val
NM_006005.3:c.943C>G MANE Select	NP_005996.2:p.Leu315Val
XM_017008586.1:c.952C>G	XP_016864075.1:p.Leu318Val