Canonical Allele Identifier: CA2669826219

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291887-C-CGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291887_6291888insGA , CM000666.2:g.6291887_6291888insGA	GRCh38
NC_000004.11:g.6293614_6293615insGA , CM000666.1:g.6293614_6293615insGA	GRCh37
NC_000004.10:g.6344515_6344516insGA	NCBI36
NG_011700.1:g.27038_27039insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.632-30_632-29insGA	ENSP00000507852.1:n.632-30_632-29insGA
ENST00000683395.1:c.609-30_609-29insGA
ENST00000684087.1:c.632-30_632-29insGA	ENSP00000506978.1:n.632-30_632-29insGA
ENST00000506362.2:c.383-30_383-29insGA	ENSP00000424103.2:n.383-30_383-29insGA
ENST00000673642.1:c.431-30_431-29insGA	ENSP00000501242.1:n.431-30_431-29insGA
ENST00000673991.1:c.632-30_632-29insGA	ENSP00000501033.1:n.632-30_632-29insGA
ENST00000226760.5:c.632-30_632-29insGA MANE Select	ENSP00000226760.1:n.632-30_632-29insGA
ENST00000503569.5:c.632-30_632-29insGA	ENSP00000423337.1:n.632-30_632-29insGA
ENST00000506362.1:c.229-30_229-29insGA
ENST00000507765.1:n.817-30_817-29insGA
NM_001145853.1:c.632-30_632-29insGA	NP_001139325.1:n.632-30_632-29insGA
NM_006005.3:c.632-30_632-29insGA MANE Select	NP_005996.2:n.632-30_632-29insGA
XM_017008586.1:c.641-30_641-29insGA	XP_016864075.1:n.641-30_641-29insGA