Canonical Allele Identifier: CA438368363

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301568-T-C
• MyVariant Identifiers: chr4:g.6303295T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301568T>C , CM000666.2:g.6301568T>C	GRCh38
NC_000004.11:g.6303295T>C , CM000666.1:g.6303295T>C	GRCh37
NC_000004.10:g.6354196T>C	NCBI36
NG_011700.1:g.36719T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1809T>C	ENSP00000507852.1:p.Ser603=
ENST00000683395.1:c.1750T>C
ENST00000684087.1:c.1773T>C	ENSP00000506978.1:p.Ser591=
ENST00000506362.2:c.1524T>C	ENSP00000424103.2:p.Ser508=
ENST00000673642.1:c.1432T>C	ENSP00000501242.1:n.1432T>C
ENST00000673991.1:c.1809T>C	ENSP00000501033.1:p.Ser603=
ENST00000226760.5:c.1773T>C MANE Select	ENSP00000226760.1:p.Ser591=
ENST00000503569.5:c.1773T>C	ENSP00000423337.1:p.Ser591=
ENST00000507765.1:n.1958T>C
NM_001145853.1:c.1773T>C	NP_001139325.1:p.Ser591=
NM_006005.3:c.1773T>C MANE Select	NP_005996.2:p.Ser591=
XM_017008586.1:c.1782T>C	XP_016864075.1:p.Ser594=