Canonical Allele Identifier: CA2760283966

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291495_6291496insACT , CM000666.2:g.6291495_6291496insACT	GRCh38
NC_000004.11:g.6293222_6293223insACT , CM000666.1:g.6293222_6293223insACT	GRCh37
NC_000004.10:g.6344123_6344124insACT	NCBI36
NG_011700.1:g.26646_26647insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+128_631+129insACT	ENSP00000507852.1:n.631+128_631+129insACT
ENST00000683395.1:c.608+141_608+142insACT
ENST00000684087.1:c.631+128_631+129insACT	ENSP00000506978.1:n.631+128_631+129insACT
ENST00000684700.1:c.*54_*55insACT	ENSP00000507806.1:n.*54_*55insACT
ENST00000506362.2:c.382+128_382+129insACT	ENSP00000424103.2:n.382+128_382+129insACT
ENST00000673642.1:c.430+128_430+129insACT	ENSP00000501242.1:n.430+128_430+129insACT
ENST00000673991.1:c.631+128_631+129insACT	ENSP00000501033.1:n.631+128_631+129insACT
ENST00000226760.5:c.631+128_631+129insACT MANE Select	ENSP00000226760.1:n.631+128_631+129insACT
ENST00000503569.5:c.631+128_631+129insACT	ENSP00000423337.1:n.631+128_631+129insACT
ENST00000506362.1:c.228+128_228+129insACT
ENST00000507765.1:n.816+128_816+129insACT
NM_001145853.1:c.631+128_631+129insACT	NP_001139325.1:n.631+128_631+129insACT
NM_006005.3:c.631+128_631+129insACT MANE Select	NP_005996.2:n.631+128_631+129insACT
XM_017008586.1:c.640+128_640+129insACT	XP_016864075.1:n.640+128_640+129insACT