Canonical Allele Identifier: CA2669826192

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291842-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291843_6291844del , CM000666.2:g.6291843_6291844del	GRCh38
NC_000004.11:g.6293570_6293571del , CM000666.1:g.6293570_6293571del	GRCh37
NC_000004.10:g.6344471_6344472del	NCBI36
NG_011700.1:g.26994_26995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.632-74_632-73del	ENSP00000507852.1:n.632-74_632-73del
ENST00000683395.1:c.609-74_609-73del
ENST00000684087.1:c.632-74_632-73del	ENSP00000506978.1:n.632-74_632-73del
ENST00000506362.2:c.383-74_383-73del	ENSP00000424103.2:n.383-74_383-73del
ENST00000673642.1:c.431-74_431-73del	ENSP00000501242.1:n.431-74_431-73del
ENST00000673991.1:c.632-74_632-73del	ENSP00000501033.1:n.632-74_632-73del
ENST00000226760.5:c.632-74_632-73del MANE Select	ENSP00000226760.1:n.632-74_632-73del
ENST00000503569.5:c.632-74_632-73del	ENSP00000423337.1:n.632-74_632-73del
ENST00000506362.1:c.229-74_229-73del
ENST00000507765.1:n.817-74_817-73del
NM_001145853.1:c.632-74_632-73del	NP_001139325.1:n.632-74_632-73del
NM_006005.3:c.632-74_632-73del MANE Select	NP_005996.2:n.632-74_632-73del
XM_017008586.1:c.641-74_641-73del	XP_016864075.1:n.641-74_641-73del