Canonical Allele Identifier: CA1435772276

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300844_6300848delinsTCTAC , CM000666.2:g.6300844_6300848delinsTCTAC	GRCh38
NC_000004.11:g.6302571_6302575delinsTCTAC , CM000666.1:g.6302571_6302575delinsTCTAC	GRCh37
NC_000004.10:g.6353472_6353476delinsTCTAC	NCBI36
NG_011700.1:g.35995_35999delinsTCTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1085_1089delinsTCTAC	ENSP00000507852.1:p.Phe362=
ENST00000683395.1:c.1026_1030delinsTCTAC
ENST00000684087.1:c.1049_1053delinsTCTAC	ENSP00000506978.1:p.Phe350=
ENST00000506362.2:c.800_804delinsTCTAC	ENSP00000424103.2:p.Phe267=
ENST00000673642.1:c.708_712delinsTCTAC	ENSP00000501242.1:p.Leu236=
ENST00000673991.1:c.1085_1089delinsTCTAC	ENSP00000501033.1:p.Phe362=
ENST00000226760.5:c.1049_1053delinsTCTAC MANE Select	ENSP00000226760.1:p.Phe350=
ENST00000503569.5:c.1049_1053delinsTCTAC	ENSP00000423337.1:p.Phe350=
ENST00000506362.1:c.682_686delinsTCTAC
ENST00000507765.1:n.1234_1238delinsTCTAC
NM_001145853.1:c.1049_1053delinsTCTAC	NP_001139325.1:p.Phe350=
NM_006005.3:c.1049_1053delinsTCTAC MANE Select	NP_005996.2:p.Phe350=
XM_017008586.1:c.1058_1062delinsTCTAC	XP_016864075.1:p.Phe353=