Canonical Allele Identifier: CA2760284024

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291531_6291532insA , CM000666.2:g.6291531_6291532insA	GRCh38
NC_000004.11:g.6293258_6293259insA , CM000666.1:g.6293258_6293259insA	GRCh37
NC_000004.10:g.6344159_6344160insA	NCBI36
NG_011700.1:g.26682_26683insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+164_631+165insA	ENSP00000507852.1:n.631+164_631+165insA
ENST00000683395.1:c.608+177_608+178insA
ENST00000684087.1:c.631+164_631+165insA	ENSP00000506978.1:n.631+164_631+165insA
ENST00000684700.1:c.*90_*91insA	ENSP00000507806.1:n.*90_*91insA
ENST00000506362.2:c.382+164_382+165insA	ENSP00000424103.2:n.382+164_382+165insA
ENST00000673642.1:c.430+164_430+165insA	ENSP00000501242.1:n.430+164_430+165insA
ENST00000673991.1:c.631+164_631+165insA	ENSP00000501033.1:n.631+164_631+165insA
ENST00000226760.5:c.631+164_631+165insA MANE Select	ENSP00000226760.1:n.631+164_631+165insA
ENST00000503569.5:c.631+164_631+165insA	ENSP00000423337.1:n.631+164_631+165insA
ENST00000506362.1:c.228+164_228+165insA
ENST00000507765.1:n.816+164_816+165insA
NM_001145853.1:c.631+164_631+165insA	NP_001139325.1:n.631+164_631+165insA
NM_006005.3:c.631+164_631+165insA MANE Select	NP_005996.2:n.631+164_631+165insA
XM_017008586.1:c.640+164_640+165insA	XP_016864075.1:n.640+164_640+165insA