Canonical Allele Identifier: CA438368081

Gene: WFS1

Linked Data

• dbSNP Id: rs1457578606
• gnomAD v2: 4-6302650-C-T
• gnomAD v4: 4-6300923-C-T
• MyVariant Identifiers: chr4:g.6302650C>T (hg19) ; chr4:g.6300923C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300923C>T , CM000666.2:g.6300923C>T	GRCh38
NC_000004.11:g.6302650C>T , CM000666.1:g.6302650C>T	GRCh37
NC_000004.10:g.6353551C>T	NCBI36
NG_011700.1:g.36074C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1164C>T	ENSP00000507852.1:p.Thr388=
ENST00000683395.1:c.1105C>T
ENST00000684087.1:c.1128C>T	ENSP00000506978.1:p.Thr376=
ENST00000506362.2:c.879C>T	ENSP00000424103.2:p.Thr293=
ENST00000673642.1:c.787C>T	ENSP00000501242.1:p.Pro263Ser
ENST00000673991.1:c.1164C>T	ENSP00000501033.1:p.Thr388=
ENST00000226760.5:c.1128C>T MANE Select	ENSP00000226760.1:p.Thr376=
ENST00000503569.5:c.1128C>T	ENSP00000423337.1:p.Thr376=
ENST00000507765.1:n.1313C>T
NM_001145853.1:c.1128C>T	NP_001139325.1:p.Thr376=
NM_006005.3:c.1128C>T MANE Select	NP_005996.2:p.Thr376=
XM_017008586.1:c.1137C>T	XP_016864075.1:p.Thr379=