Canonical Allele Identifier: CA356174369

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300955-A-G
• MyVariant Identifiers: chr4:g.6302682A>G (hg19) ; chr4:g.6300955A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300955A>G , CM000666.2:g.6300955A>G	GRCh38
NC_000004.11:g.6302682A>G , CM000666.1:g.6302682A>G	GRCh37
NC_000004.10:g.6353583A>G	NCBI36
NG_011700.1:g.36106A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1196A>G	ENSP00000507852.1:p.Asn399Ser
ENST00000683395.1:c.1137A>G
ENST00000684087.1:c.1160A>G	ENSP00000506978.1:p.Asn387Ser
ENST00000506362.2:c.911A>G	ENSP00000424103.2:p.Asn304Ser
ENST00000673642.1:c.819A>G	ENSP00000501242.1:p.Gln273=
ENST00000673991.1:c.1196A>G	ENSP00000501033.1:p.Asn399Ser
ENST00000226760.5:c.1160A>G MANE Select	ENSP00000226760.1:p.Asn387Ser
ENST00000503569.5:c.1160A>G	ENSP00000423337.1:p.Asn387Ser
ENST00000507765.1:n.1345A>G
NM_001145853.1:c.1160A>G	NP_001139325.1:p.Asn387Ser
NM_006005.3:c.1160A>G MANE Select	NP_005996.2:p.Asn387Ser
XM_017008586.1:c.1169A>G	XP_016864075.1:p.Asn390Ser