Canonical Allele Identifier: CA1435772133

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301967_6301970delinsGTTC , CM000666.2:g.6301967_6301970delinsGTTC	GRCh38
NC_000004.11:g.6303694_6303697delinsGTTC , CM000666.1:g.6303694_6303697delinsGTTC	GRCh37
NC_000004.10:g.6354595_6354598delinsGTTC	NCBI36
NG_011700.1:g.37118_37121delinsGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2208_2211delinsGTTC	ENSP00000507852.1:p.Pro736=
ENST00000683395.1:c.2149_2152delinsGTTC
ENST00000684087.1:c.2172_2175delinsGTTC	ENSP00000506978.1:p.Pro724=
ENST00000506362.2:c.1923_1926delinsGTTC	ENSP00000424103.2:p.Pro641=
ENST00000673642.1:c.1831_1834delinsGTTC	ENSP00000501242.1:n.1831_1834delinsGTTC
ENST00000673991.1:c.2208_2211delinsGTTC	ENSP00000501033.1:p.Pro736=
ENST00000226760.5:c.2172_2175delinsGTTC MANE Select	ENSP00000226760.1:p.Pro724=
ENST00000503569.5:c.2172_2175delinsGTTC	ENSP00000423337.1:p.Pro724=
ENST00000507765.1:n.2357_2360delinsGTTC
NM_001145853.1:c.2172_2175delinsGTTC	NP_001139325.1:p.Pro724=
NM_006005.3:c.2172_2175delinsGTTC MANE Select	NP_005996.2:p.Pro724=
XM_017008586.1:c.2181_2184delinsGTTC	XP_016864075.1:p.Pro727=