Canonical Allele Identifier: CA2760283992

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291510_6291511insACA , CM000666.2:g.6291510_6291511insACA	GRCh38
NC_000004.11:g.6293237_6293238insACA , CM000666.1:g.6293237_6293238insACA	GRCh37
NC_000004.10:g.6344138_6344139insACA	NCBI36
NG_011700.1:g.26661_26662insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+143_631+144insACA	ENSP00000507852.1:n.631+143_631+144insACA
ENST00000683395.1:c.608+156_608+157insACA
ENST00000684087.1:c.631+143_631+144insACA	ENSP00000506978.1:n.631+143_631+144insACA
ENST00000684700.1:c.*69_*70insACA	ENSP00000507806.1:n.*69_*70insACA
ENST00000506362.2:c.382+143_382+144insACA	ENSP00000424103.2:n.382+143_382+144insACA
ENST00000673642.1:c.430+143_430+144insACA	ENSP00000501242.1:n.430+143_430+144insACA
ENST00000673991.1:c.631+143_631+144insACA	ENSP00000501033.1:n.631+143_631+144insACA
ENST00000226760.5:c.631+143_631+144insACA MANE Select	ENSP00000226760.1:n.631+143_631+144insACA
ENST00000503569.5:c.631+143_631+144insACA	ENSP00000423337.1:n.631+143_631+144insACA
ENST00000506362.1:c.228+143_228+144insACA
ENST00000507765.1:n.816+143_816+144insACA
NM_001145853.1:c.631+143_631+144insACA	NP_001139325.1:n.631+143_631+144insACA
NM_006005.3:c.631+143_631+144insACA MANE Select	NP_005996.2:n.631+143_631+144insACA
XM_017008586.1:c.640+143_640+144insACA	XP_016864075.1:n.640+143_640+144insACA