Canonical Allele Identifier: CA2669843474

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301971-TTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301974_6301976del , CM000666.2:g.6301974_6301976del	GRCh38
NC_000004.11:g.6303701_6303703del , CM000666.1:g.6303701_6303703del	GRCh37
NC_000004.10:g.6354602_6354604del	NCBI36
NG_011700.1:g.37125_37127del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2215_2217del	ENSP00000507852.1:p.Ile739del
ENST00000683395.1:c.2156_2158del
ENST00000684087.1:c.2179_2181del	ENSP00000506978.1:p.Ile727del
ENST00000506362.2:c.1930_1932del	ENSP00000424103.2:p.Ile644del
ENST00000673642.1:c.1838_1840del	ENSP00000501242.1:n.1838_1840del
ENST00000673991.1:c.2215_2217del	ENSP00000501033.1:p.Ile739del
ENST00000226760.5:c.2179_2181del MANE Select	ENSP00000226760.1:p.Ile727del
ENST00000503569.5:c.2179_2181del	ENSP00000423337.1:p.Ile727del
ENST00000507765.1:n.2364_2366del
NM_001145853.1:c.2179_2181del	NP_001139325.1:p.Ile727del
NM_006005.3:c.2179_2181del MANE Select	NP_005996.2:p.Ile727del
XM_017008586.1:c.2188_2190del	XP_016864075.1:p.Ile730del