Canonical Allele Identifier: CA2760284041

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291541_6291542insA , CM000666.2:g.6291541_6291542insA	GRCh38
NC_000004.11:g.6293268_6293269insA , CM000666.1:g.6293268_6293269insA	GRCh37
NC_000004.10:g.6344169_6344170insA	NCBI36
NG_011700.1:g.26692_26693insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+174_631+175insA	ENSP00000507852.1:n.631+174_631+175insA
ENST00000683395.1:c.608+187_608+188insA
ENST00000684087.1:c.631+174_631+175insA	ENSP00000506978.1:n.631+174_631+175insA
ENST00000684700.1:c.*100_*101insA	ENSP00000507806.1:n.*100_*101insA
ENST00000506362.2:c.382+174_382+175insA	ENSP00000424103.2:n.382+174_382+175insA
ENST00000673642.1:c.430+174_430+175insA	ENSP00000501242.1:n.430+174_430+175insA
ENST00000673991.1:c.631+174_631+175insA	ENSP00000501033.1:n.631+174_631+175insA
ENST00000226760.5:c.631+174_631+175insA MANE Select	ENSP00000226760.1:n.631+174_631+175insA
ENST00000503569.5:c.631+174_631+175insA	ENSP00000423337.1:n.631+174_631+175insA
ENST00000506362.1:c.228+174_228+175insA
ENST00000507765.1:n.816+174_816+175insA
NM_001145853.1:c.631+174_631+175insA	NP_001139325.1:n.631+174_631+175insA
NM_006005.3:c.631+174_631+175insA MANE Select	NP_005996.2:n.631+174_631+175insA
XM_017008586.1:c.640+174_640+175insA	XP_016864075.1:n.640+174_640+175insA