Canonical Allele Identifier: CA1435772264

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300840_6300843delinsATCT , CM000666.2:g.6300840_6300843delinsATCT	GRCh38
NC_000004.11:g.6302567_6302570delinsATCT , CM000666.1:g.6302567_6302570delinsATCT	GRCh37
NC_000004.10:g.6353468_6353471delinsATCT	NCBI36
NG_011700.1:g.35991_35994delinsATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1081_1084delinsATCT	ENSP00000507852.1:p.Ile361=
ENST00000683395.1:c.1022_1025delinsATCT
ENST00000684087.1:c.1045_1048delinsATCT	ENSP00000506978.1:p.Ile349=
ENST00000506362.2:c.796_799delinsATCT	ENSP00000424103.2:p.Ile266=
ENST00000673642.1:c.704_707delinsATCT	ENSP00000501242.1:p.His235=
ENST00000673991.1:c.1081_1084delinsATCT	ENSP00000501033.1:p.Ile361=
ENST00000226760.5:c.1045_1048delinsATCT MANE Select	ENSP00000226760.1:p.Ile349=
ENST00000503569.5:c.1045_1048delinsATCT	ENSP00000423337.1:p.Ile349=
ENST00000506362.1:c.678_681delinsATCT
ENST00000507765.1:n.1230_1233delinsATCT
NM_001145853.1:c.1045_1048delinsATCT	NP_001139325.1:p.Ile349=
NM_006005.3:c.1045_1048delinsATCT MANE Select	NP_005996.2:p.Ile349=
XM_017008586.1:c.1054_1057delinsATCT	XP_016864075.1:p.Ile352=