Canonical Allele Identifier: CA2669843448

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301483-A-ACTTCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301493_6301498dup , CM000666.2:g.6301493_6301498dup	GRCh38
NC_000004.11:g.6303220_6303225dup , CM000666.1:g.6303220_6303225dup	GRCh37
NC_000004.10:g.6354121_6354126dup	NCBI36
NG_011700.1:g.36644_36649dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1734_1739dup	ENSP00000507852.1:p.Phe580_Ala581insLeuPhe
ENST00000683395.1:c.1675_1680dup
ENST00000684087.1:c.1698_1703dup	ENSP00000506978.1:p.Phe568_Ala569insLeuPhe
ENST00000506362.2:c.1449_1454dup	ENSP00000424103.2:p.Phe485_Ala486insLeuPhe
ENST00000673642.1:c.1357_1362dup	ENSP00000501242.1:n.1357_1362dup
ENST00000673991.1:c.1734_1739dup	ENSP00000501033.1:p.Phe580_Ala581insLeuPhe
ENST00000226760.5:c.1698_1703dup MANE Select	ENSP00000226760.1:p.Phe568_Ala569insLeuPhe
ENST00000503569.5:c.1698_1703dup	ENSP00000423337.1:p.Phe568_Ala569insLeuPhe
ENST00000507765.1:n.1883_1888dup
NM_001145853.1:c.1698_1703dup	NP_001139325.1:p.Phe568_Ala569insLeuPhe
NM_006005.3:c.1698_1703dup MANE Select	NP_005996.2:p.Phe568_Ala569insLeuPhe
XM_017008586.1:c.1707_1712dup	XP_016864075.1:p.Phe571_Ala572insLeuPhe