Canonical Allele Identifier: CA2669826086

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291499-T-TCCTCACAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291499_6291500insCCTCACAGG , CM000666.2:g.6291499_6291500insCCTCACAGG	GRCh38
NC_000004.11:g.6293226_6293227insCCTCACAGG , CM000666.1:g.6293226_6293227insCCTCACAGG	GRCh37
NC_000004.10:g.6344127_6344128insCCTCACAGG	NCBI36
NG_011700.1:g.26650_26651insCCTCACAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+132_631+133insCCTCACAGG	ENSP00000507852.1:n.631+132_631+133insCCTCACAGG
ENST00000683395.1:c.608+145_608+146insCCTCACAGG
ENST00000684087.1:c.631+132_631+133insCCTCACAGG	ENSP00000506978.1:n.631+132_631+133insCCTCACAGG
ENST00000684700.1:c.*58_*59insCCTCACAGG	ENSP00000507806.1:n.*58_*59insCCTCACAGG
ENST00000506362.2:c.382+132_382+133insCCTCACAGG	ENSP00000424103.2:n.382+132_382+133insCCTCACAGG
ENST00000673642.1:c.430+132_430+133insCCTCACAGG	ENSP00000501242.1:n.430+132_430+133insCCTCACAGG
ENST00000673991.1:c.631+132_631+133insCCTCACAGG	ENSP00000501033.1:n.631+132_631+133insCCTCACAGG
ENST00000226760.5:c.631+132_631+133insCCTCACAGG MANE Select	ENSP00000226760.1:n.631+132_631+133insCCTCACAGG
ENST00000503569.5:c.631+132_631+133insCCTCACAGG	ENSP00000423337.1:n.631+132_631+133insCCTCACAGG
ENST00000506362.1:c.228+132_228+133insCCTCACAGG
ENST00000507765.1:n.816+132_816+133insCCTCACAGG
NM_001145853.1:c.631+132_631+133insCCTCACAGG	NP_001139325.1:n.631+132_631+133insCCTCACAGG
NM_006005.3:c.631+132_631+133insCCTCACAGG MANE Select	NP_005996.2:n.631+132_631+133insCCTCACAGG
XM_017008586.1:c.640+132_640+133insCCTCACAGG	XP_016864075.1:n.640+132_640+133insCCTCACAGG