Canonical Allele Identifier: CA2669843034

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300517-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300518_6300519dup , CM000666.2:g.6300518_6300519dup	GRCh38
NC_000004.11:g.6302245_6302246dup , CM000666.1:g.6302245_6302246dup	GRCh37
NC_000004.10:g.6353146_6353147dup	NCBI36
NG_011700.1:g.35669_35670dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-139_898-138dup	ENSP00000507852.1:n.898-139_898-138dup
ENST00000683395.1:c.839-139_839-138dup
ENST00000684087.1:c.862-139_862-138dup	ENSP00000506978.1:n.862-139_862-138dup
ENST00000506362.2:c.613-139_613-138dup	ENSP00000424103.2:n.613-139_613-138dup
ENST00000673642.1:c.661-279_661-278dup	ENSP00000501242.1:n.661-279_661-278dup
ENST00000673991.1:c.898-139_898-138dup	ENSP00000501033.1:n.898-139_898-138dup
ENST00000226760.5:c.862-139_862-138dup MANE Select	ENSP00000226760.1:n.862-139_862-138dup
ENST00000503569.5:c.862-139_862-138dup	ENSP00000423337.1:n.862-139_862-138dup
ENST00000506362.1:c.495-139_495-138dup
ENST00000507765.1:n.1047-139_1047-138dup
ENST00000513395.1:n.420-139_420-138dup
NM_001145853.1:c.862-139_862-138dup	NP_001139325.1:n.862-139_862-138dup
NM_006005.3:c.862-139_862-138dup MANE Select	NP_005996.2:n.862-139_862-138dup
XM_017008586.1:c.871-139_871-138dup	XP_016864075.1:n.871-139_871-138dup