Canonical Allele Identifier: CA2586973606

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300841_6300842delinsAG , CM000666.2:g.6300841_6300842delinsAG	GRCh38
NC_000004.11:g.6302568_6302569delinsAG , CM000666.1:g.6302568_6302569delinsAG	GRCh37
NC_000004.10:g.6353469_6353470delinsAG	NCBI36
NG_011700.1:g.35992_35993delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1082_1083delinsAG	ENSP00000507852.1:p.Ile361Lys
ENST00000683395.1:c.1023_1024delinsAG
ENST00000684087.1:c.1046_1047delinsAG	ENSP00000506978.1:p.Ile349Lys
ENST00000506362.2:c.797_798delinsAG	ENSP00000424103.2:p.Ile266Lys
ENST00000673642.1:c.705_706delinsAG	ENSP00000501242.1:p.His235_Leu236delinsGlnVal
ENST00000673991.1:c.1082_1083delinsAG	ENSP00000501033.1:p.Ile361Lys
ENST00000226760.5:c.1046_1047delinsAG MANE Select	ENSP00000226760.1:p.Ile349Lys
ENST00000503569.5:c.1046_1047delinsAG	ENSP00000423337.1:p.Ile349Lys
ENST00000506362.1:c.679_680delinsAG
ENST00000507765.1:n.1231_1232delinsAG
NM_001145853.1:c.1046_1047delinsAG	NP_001139325.1:p.Ile349Lys
NM_006005.3:c.1046_1047delinsAG MANE Select	NP_005996.2:p.Ile349Lys
XM_017008586.1:c.1055_1056delinsAG	XP_016864075.1:p.Ile352Lys