Canonical Allele Identifier: CA91798209

Gene: WFS1

Linked Data

• dbSNP Id: rs952593169
• gnomAD v2: 4-6304454-T-G
• gnomAD v3: 4-6302727-T-G
• gnomAD v4: 4-6302727-T-G
• MyVariant Identifiers: chr4:g.6304454T>G (hg19) ; chr4:g.6302727T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302727T>G , CM000666.2:g.6302727T>G	GRCh38
NC_000004.11:g.6304454T>G , CM000666.1:g.6304454T>G	GRCh37
NC_000004.10:g.6355355T>G	NCBI36
NG_011700.1:g.37878T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*259T>G	ENSP00000507852.1:n.*259T>G
ENST00000683395.1:c.2909T>G
ENST00000684087.1:c.*259T>G	ENSP00000506978.1:n.*259T>G
ENST00000506362.2:c.*259T>G	ENSP00000424103.2:n.*259T>G
ENST00000673991.1:c.*259T>G	ENSP00000501033.1:n.*259T>G
ENST00000226760.5:c.*259T>G MANE Select	ENSP00000226760.1:n.*259T>G
ENST00000503569.5:c.*259T>G	ENSP00000423337.1:n.*259T>G
ENST00000507765.1:n.3117T>G
NM_001145853.1:c.*259T>G	NP_001139325.1:n.*259T>G
NM_006005.3:c.*259T>G MANE Select	NP_005996.2:n.*259T>G
XM_017008586.1:c.*259T>G	XP_016864075.1:n.*259T>G