Canonical Allele Identifier: CA2760283944

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291486_6291487insA , CM000666.2:g.6291486_6291487insA	GRCh38
NC_000004.11:g.6293213_6293214insA , CM000666.1:g.6293213_6293214insA	GRCh37
NC_000004.10:g.6344114_6344115insA	NCBI36
NG_011700.1:g.26637_26638insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+119_631+120insA	ENSP00000507852.1:n.631+119_631+120insA
ENST00000683395.1:c.608+132_608+133insA
ENST00000684087.1:c.631+119_631+120insA	ENSP00000506978.1:n.631+119_631+120insA
ENST00000684700.1:c.*45_*46insA	ENSP00000507806.1:n.*45_*46insA
ENST00000506362.2:c.382+119_382+120insA	ENSP00000424103.2:n.382+119_382+120insA
ENST00000673642.1:c.430+119_430+120insA	ENSP00000501242.1:n.430+119_430+120insA
ENST00000673991.1:c.631+119_631+120insA	ENSP00000501033.1:n.631+119_631+120insA
ENST00000226760.5:c.631+119_631+120insA MANE Select	ENSP00000226760.1:n.631+119_631+120insA
ENST00000503569.5:c.631+119_631+120insA	ENSP00000423337.1:n.631+119_631+120insA
ENST00000506362.1:c.228+119_228+120insA
ENST00000507765.1:n.816+119_816+120insA
NM_001145853.1:c.631+119_631+120insA	NP_001139325.1:n.631+119_631+120insA
NM_006005.3:c.631+119_631+120insA MANE Select	NP_005996.2:n.631+119_631+120insA
XM_017008586.1:c.640+119_640+120insA	XP_016864075.1:n.640+119_640+120insA