Canonical Allele Identifier: CA2586973634

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301519-CCGGCCTGGCCCTGGTGGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301522_6301539del , CM000666.2:g.6301522_6301539del	GRCh38
NC_000004.11:g.6303249_6303266del , CM000666.1:g.6303249_6303266del	GRCh37
NC_000004.10:g.6354150_6354167del	NCBI36
NG_011700.1:g.36673_36690del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.1763_1780del	ENSP00000507852.1:p.Gly588_Gly593del
ENST00000683395.1:c.1704_1721del
ENST00000684087.1:c.1727_1744del	ENSP00000506978.1:p.Gly576_Gly581del
ENST00000506362.2:c.1478_1495del	ENSP00000424103.2:p.Gly493_Gly498del
ENST00000673642.1:c.1386_1403del	ENSP00000501242.1:n.1386_1403del
ENST00000673991.1:c.1763_1780del	ENSP00000501033.1:p.Gly588_Gly593del
ENST00000226760.5:c.1727_1744del MANE Select	ENSP00000226760.1:p.Gly576_Gly581del
ENST00000503569.5:c.1727_1744del	ENSP00000423337.1:p.Gly576_Gly581del
ENST00000507765.1:n.1912_1929del
NM_001145853.1:c.1727_1744del	NP_001139325.1:p.Gly576_Gly581del
NM_006005.3:c.1727_1744del MANE Select	NP_005996.2:p.Gly576_Gly581del
XM_017008586.1:c.1736_1753del	XP_016864075.1:p.Gly579_Gly584del