Canonical Allele Identifier: CA3030547169

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291530_6291537del , CM000666.2:g.6291530_6291537del	GRCh38
NC_000004.11:g.6293257_6293264del , CM000666.1:g.6293257_6293264del	GRCh37
NC_000004.10:g.6344158_6344165del	NCBI36
NG_011700.1:g.26681_26688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+163_631+170del	ENSP00000507852.1:n.631+163_631+170del
ENST00000683395.1:c.608+176_608+183del
ENST00000684087.1:c.631+163_631+170del	ENSP00000506978.1:n.631+163_631+170del
ENST00000684700.1:c.*89_*96del	ENSP00000507806.1:n.*89_*96del
ENST00000506362.2:c.382+163_382+170del	ENSP00000424103.2:n.382+163_382+170del
ENST00000673642.1:c.430+163_430+170del	ENSP00000501242.1:n.430+163_430+170del
ENST00000673991.1:c.631+163_631+170del	ENSP00000501033.1:n.631+163_631+170del
ENST00000226760.5:c.631+163_631+170del MANE Select	ENSP00000226760.1:n.631+163_631+170del
ENST00000503569.5:c.631+163_631+170del	ENSP00000423337.1:n.631+163_631+170del
ENST00000506362.1:c.228+163_228+170del
ENST00000507765.1:n.816+163_816+170del
NM_001145853.1:c.631+163_631+170del	NP_001139325.1:n.631+163_631+170del
NM_006005.3:c.631+163_631+170del MANE Select	NP_005996.2:n.631+163_631+170del
XM_017008586.1:c.640+163_640+170del	XP_016864075.1:n.640+163_640+170del