Canonical Allele Identifier: CA2669843447

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301471-C-CCTCCATCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301474_6301482dup , CM000666.2:g.6301474_6301482dup	GRCh38
NC_000004.11:g.6303201_6303209dup , CM000666.1:g.6303201_6303209dup	GRCh37
NC_000004.10:g.6354102_6354110dup	NCBI36
NG_011700.1:g.36625_36633dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1715_1723dup	ENSP00000507852.1:p.Gly574_Tyr575insSerIleGly
ENST00000683395.1:c.1656_1664dup
ENST00000684087.1:c.1679_1687dup	ENSP00000506978.1:p.Gly562_Tyr563insSerIleGly
ENST00000506362.2:c.1430_1438dup	ENSP00000424103.2:p.Gly479_Tyr480insSerIleGly
ENST00000673642.1:c.1338_1346dup	ENSP00000501242.1:n.1338_1346dup
ENST00000673991.1:c.1715_1723dup	ENSP00000501033.1:p.Gly574_Tyr575insSerIleGly
ENST00000226760.5:c.1679_1687dup MANE Select	ENSP00000226760.1:p.Gly562_Tyr563insSerIleGly
ENST00000503569.5:c.1679_1687dup	ENSP00000423337.1:p.Gly562_Tyr563insSerIleGly
ENST00000507765.1:n.1864_1872dup
NM_001145853.1:c.1679_1687dup	NP_001139325.1:p.Gly562_Tyr563insSerIleGly
NM_006005.3:c.1679_1687dup MANE Select	NP_005996.2:p.Gly562_Tyr563insSerIleGly
XM_017008586.1:c.1688_1696dup	XP_016864075.1:p.Gly565_Tyr566insSerIleGly