Canonical Allele Identifier: CA1435773324

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302898_6302900delinsATT , CM000666.2:g.6302898_6302900delinsATT	GRCh38
NC_000004.11:g.6304625_6304627delinsATT , CM000666.1:g.6304625_6304627delinsATT	GRCh37
NC_000004.10:g.6355526_6355528delinsATT	NCBI36
NG_011700.1:g.38049_38051delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*430_*432delinsATT	ENSP00000507852.1:n.*430_*432delinsATT
ENST00000683395.1:c.3080_3082delinsATT
ENST00000684087.1:c.*430_*432delinsATT	ENSP00000506978.1:n.*430_*432delinsATT
ENST00000673991.1:c.*430_*432delinsATT	ENSP00000501033.1:n.*430_*432delinsATT
ENST00000226760.5:c.*430_*432delinsATT MANE Select	ENSP00000226760.1:n.*430_*432delinsATT
ENST00000507765.1:n.3288_3290delinsATT
NM_001145853.1:c.*430_*432delinsATT	NP_001139325.1:n.*430_*432delinsATT
NM_006005.3:c.*430_*432delinsATT MANE Select	NP_005996.2:n.*430_*432delinsATT
XM_017008586.1:c.*430_*432delinsATT	XP_016864075.1:n.*430_*432delinsATT
XR_001741566.2:n.2045_2047delinsAAT