Canonical Allele Identifier: CA179653

Gene: WFS1

Linked Data

• ClinVar Variation Id: 166591
• ClinVar RCV Id: RCV000152678 ; RCV000295433 ; RCV000389673 ; RCV000756924 ; RCV003126549 ; RCV002498719
• dbSNP Id: rs35789242
• ExAC: 4:6303052 C / T
• gnomAD v2: 4-6303052-C-T
• gnomAD v3: 4-6301325-C-T
• gnomAD v4: 4-6301325-C-T
• MyVariant Identifiers: chr4:g.6303052C>T (hg19) ; chr4:g.6301325C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301325C>T , CM000666.2:g.6301325C>T	GRCh38
NC_000004.11:g.6303052C>T , CM000666.1:g.6303052C>T	GRCh37
NC_000004.10:g.6353953C>T	NCBI36
NG_011700.1:g.36476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1566C>T	ENSP00000507852.1:p.Tyr522=
ENST00000683395.1:c.1507C>T
ENST00000684087.1:c.1530C>T	ENSP00000506978.1:p.Tyr510=
ENST00000506362.2:c.1281C>T	ENSP00000424103.2:p.Tyr427=
ENST00000673642.1:c.1189C>T	ENSP00000501242.1:p.Pro397Ser
ENST00000673991.1:c.1566C>T	ENSP00000501033.1:p.Tyr522=
ENST00000226760.5:c.1530C>T MANE Select	ENSP00000226760.1:p.Tyr510=
ENST00000503569.5:c.1530C>T	ENSP00000423337.1:p.Tyr510=
ENST00000507765.1:n.1715C>T
NM_001145853.1:c.1530C>T	NP_001139325.1:p.Tyr510=
NM_006005.3:c.1530C>T MANE Select	NP_005996.2:p.Tyr510=
XM_017008586.1:c.1539C>T	XP_016864075.1:p.Tyr513=