Canonical Allele Identifier: CA2760284005

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291516_6291517insACA , CM000666.2:g.6291516_6291517insACA	GRCh38
NC_000004.11:g.6293243_6293244insACA , CM000666.1:g.6293243_6293244insACA	GRCh37
NC_000004.10:g.6344144_6344145insACA	NCBI36
NG_011700.1:g.26667_26668insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+149_631+150insACA	ENSP00000507852.1:n.631+149_631+150insACA
ENST00000683395.1:c.608+162_608+163insACA
ENST00000684087.1:c.631+149_631+150insACA	ENSP00000506978.1:n.631+149_631+150insACA
ENST00000684700.1:c.*75_*76insACA	ENSP00000507806.1:n.*75_*76insACA
ENST00000506362.2:c.382+149_382+150insACA	ENSP00000424103.2:n.382+149_382+150insACA
ENST00000673642.1:c.430+149_430+150insACA	ENSP00000501242.1:n.430+149_430+150insACA
ENST00000673991.1:c.631+149_631+150insACA	ENSP00000501033.1:n.631+149_631+150insACA
ENST00000226760.5:c.631+149_631+150insACA MANE Select	ENSP00000226760.1:n.631+149_631+150insACA
ENST00000503569.5:c.631+149_631+150insACA	ENSP00000423337.1:n.631+149_631+150insACA
ENST00000506362.1:c.228+149_228+150insACA
ENST00000507765.1:n.816+149_816+150insACA
NM_001145853.1:c.631+149_631+150insACA	NP_001139325.1:n.631+149_631+150insACA
NM_006005.3:c.631+149_631+150insACA MANE Select	NP_005996.2:n.631+149_631+150insACA
XM_017008586.1:c.640+149_640+150insACA	XP_016864075.1:n.640+149_640+150insACA