Canonical Allele Identifier: CA2760284133

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291600_6291601insACA , CM000666.2:g.6291600_6291601insACA	GRCh38
NC_000004.11:g.6293327_6293328insACA , CM000666.1:g.6293327_6293328insACA	GRCh37
NC_000004.10:g.6344228_6344229insACA	NCBI36
NG_011700.1:g.26751_26752insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+233_631+234insACA	ENSP00000507852.1:n.631+233_631+234insACA
ENST00000683395.1:c.608+246_608+247insACA
ENST00000684087.1:c.631+233_631+234insACA	ENSP00000506978.1:n.631+233_631+234insACA
ENST00000684700.1:c.*159_*160insACA	ENSP00000507806.1:n.*159_*160insACA
ENST00000506362.2:c.382+233_382+234insACA	ENSP00000424103.2:n.382+233_382+234insACA
ENST00000673642.1:c.430+233_430+234insACA	ENSP00000501242.1:n.430+233_430+234insACA
ENST00000673991.1:c.631+233_631+234insACA	ENSP00000501033.1:n.631+233_631+234insACA
ENST00000226760.5:c.631+233_631+234insACA MANE Select	ENSP00000226760.1:n.631+233_631+234insACA
ENST00000503569.5:c.631+233_631+234insACA	ENSP00000423337.1:n.631+233_631+234insACA
ENST00000506362.1:c.228+233_228+234insACA
ENST00000507765.1:n.816+233_816+234insACA
NM_001145853.1:c.631+233_631+234insACA	NP_001139325.1:n.631+233_631+234insACA
NM_006005.3:c.631+233_631+234insACA MANE Select	NP_005996.2:n.631+233_631+234insACA
XM_017008586.1:c.640+233_640+234insACA	XP_016864075.1:n.640+233_640+234insACA