Canonical Allele Identifier: CA356178789

Gene: WFS1

Linked Data

• ClinVar Variation Id: 1375473
• ClinVar RCV Id: RCV001883361
• dbSNP Id: rs2109127724
• MyVariant Identifiers: chr4:g.6304034C>G (hg19) ; chr4:g.6302307C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302307C>G , CM000666.2:g.6302307C>G	GRCh38
NC_000004.11:g.6304034C>G , CM000666.1:g.6304034C>G	GRCh37
NC_000004.10:g.6354935C>G	NCBI36
NG_011700.1:g.37458C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2548C>G	ENSP00000507852.1:p.Pro850Ala
ENST00000683395.1:c.2489C>G
ENST00000684087.1:c.2512C>G	ENSP00000506978.1:p.Pro838Ala
ENST00000506362.2:c.2263C>G	ENSP00000424103.2:p.Pro755Ala
ENST00000673991.1:c.2548C>G	ENSP00000501033.1:p.Pro850Ala
ENST00000226760.5:c.2512C>G MANE Select	ENSP00000226760.1:p.Pro838Ala
ENST00000503569.5:c.2512C>G	ENSP00000423337.1:p.Pro838Ala
ENST00000507765.1:n.2697C>G
NM_001145853.1:c.2512C>G	NP_001139325.1:p.Pro838Ala
NM_006005.3:c.2512C>G MANE Select	NP_005996.2:p.Pro838Ala
XM_017008586.1:c.2521C>G	XP_016864075.1:p.Pro841Ala