Canonical Allele Identifier: CA549423121

Gene: WFS1

Linked Data

• dbSNP Id: rs1208367140
• gnomAD v2: 4-6292759-A-AG
• gnomAD v3: 4-6291032-A-AG
• gnomAD v4: 4-6291032-A-AG
• MyVariant Identifiers: chr4:g.6292759_6292760insG (hg19) ; chr4:g.6291032_6291033insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291032_6291033insG , CM000666.2:g.6291032_6291033insG	GRCh38
NC_000004.11:g.6292759_6292760insG , CM000666.1:g.6292759_6292760insG	GRCh37
NC_000004.10:g.6343660_6343661insG	NCBI36
NG_011700.1:g.26183_26184insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.461-165_461-164insG	ENSP00000507852.1:n.461-165_461-164insG
ENST00000683395.1:c.451-165_451-164insG
ENST00000684087.1:c.461-165_461-164insG	ENSP00000506978.1:n.461-165_461-164insG
ENST00000684700.1:c.461-165_461-164insG	ENSP00000507806.1:n.461-165_461-164insG
ENST00000506362.2:c.212-165_212-164insG	ENSP00000424103.2:n.212-165_212-164insG
ENST00000673642.1:c.260-165_260-164insG	ENSP00000501242.1:n.260-165_260-164insG
ENST00000673991.1:c.461-165_461-164insG	ENSP00000501033.1:n.461-165_461-164insG
ENST00000674051.1:c.335-165_335-164insG	ENSP00000501083.1:n.335-165_335-164insG
ENST00000226760.5:c.461-165_461-164insG MANE Select	ENSP00000226760.1:n.461-165_461-164insG
ENST00000503569.5:c.461-165_461-164insG	ENSP00000423337.1:n.461-165_461-164insG
ENST00000506362.1:c.58-165_58-164insG
ENST00000507765.1:n.646-165_646-164insG
NM_001145853.1:c.461-165_461-164insG	NP_001139325.1:n.461-165_461-164insG
NM_006005.3:c.461-165_461-164insG MANE Select	NP_005996.2:n.461-165_461-164insG
XM_017008586.1:c.470-165_470-164insG	XP_016864075.1:n.470-165_470-164insG