Canonical Allele Identifier: CA1435772955

Gene: WFS1

Linked Data

• dbSNP Id: rs1730992358
• gnomAD v4: 4-6302560-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302560C>T , CM000666.2:g.6302560C>T	GRCh38
NC_000004.11:g.6304287C>T , CM000666.1:g.6304287C>T	GRCh37
NC_000004.10:g.6355188C>T	NCBI36
NG_011700.1:g.37711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*92C>T	ENSP00000507852.1:n.*92C>T
ENST00000683395.1:c.2742C>T
ENST00000684087.1:c.*92C>T	ENSP00000506978.1:n.*92C>T
ENST00000506362.2:c.*92C>T	ENSP00000424103.2:n.*92C>T
ENST00000673991.1:c.*92C>T	ENSP00000501033.1:n.*92C>T
ENST00000226760.5:c.*92C>T MANE Select	ENSP00000226760.1:n.*92C>T
ENST00000503569.5:c.*92C>T	ENSP00000423337.1:n.*92C>T
ENST00000507765.1:n.2950C>T
NM_001145853.1:c.*92C>T	NP_001139325.1:n.*92C>T
NM_006005.3:c.*92C>T MANE Select	NP_005996.2:n.*92C>T
XM_017008586.1:c.*92C>T	XP_016864075.1:n.*92C>T