Canonical Allele Identifier: CA2839168

Gene: WFS1

Linked Data

• ClinVar Variation Id: 2727408
• ClinVar RCV Id: RCV003557191
• dbSNP Id: rs369588045
• ExAC: 4:6302482 C / T
• gnomAD v2: 4-6302482-C-T
• gnomAD v4: 4-6300755-C-T
• MyVariant Identifiers: chr4:g.6302482C>T (hg19) ; chr4:g.6300755C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300755C>T , CM000666.2:g.6300755C>T	GRCh38
NC_000004.11:g.6302482C>T , CM000666.1:g.6302482C>T	GRCh37
NC_000004.10:g.6353383C>T	NCBI36
NG_011700.1:g.35906C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.996C>T	ENSP00000507852.1:p.Pro332=
ENST00000683395.1:c.937C>T
ENST00000684087.1:c.960C>T	ENSP00000506978.1:p.Pro320=
ENST00000506362.2:c.711C>T	ENSP00000424103.2:p.Pro237=
ENST00000673642.1:c.661-42C>T	ENSP00000501242.1:n.661-42C>T
ENST00000673991.1:c.996C>T	ENSP00000501033.1:p.Pro332=
ENST00000226760.5:c.960C>T MANE Select	ENSP00000226760.1:p.Pro320=
ENST00000503569.5:c.960C>T	ENSP00000423337.1:p.Pro320=
ENST00000506362.1:c.593C>T
ENST00000507765.1:n.1145C>T
ENST00000513395.1:n.518C>T
NM_001145853.1:c.960C>T	NP_001139325.1:p.Pro320=
NM_006005.3:c.960C>T MANE Select	NP_005996.2:p.Pro320=
XM_017008586.1:c.969C>T	XP_016864075.1:p.Pro323=