Canonical Allele Identifier: CA2669843444

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301456-TGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301458_6301460del , CM000666.2:g.6301458_6301460del	GRCh38
NC_000004.11:g.6303185_6303187del , CM000666.1:g.6303185_6303187del	GRCh37
NC_000004.10:g.6354086_6354088del	NCBI36
NG_011700.1:g.36609_36611del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1699_1701del	ENSP00000507852.1:p.Gly567del
ENST00000683395.1:c.1640_1642del
ENST00000684087.1:c.1663_1665del	ENSP00000506978.1:p.Gly555del
ENST00000506362.2:c.1414_1416del	ENSP00000424103.2:p.Gly472del
ENST00000673642.1:c.1322_1324del	ENSP00000501242.1:n.1322_1324del
ENST00000673991.1:c.1699_1701del	ENSP00000501033.1:p.Gly567del
ENST00000226760.5:c.1663_1665del MANE Select	ENSP00000226760.1:p.Gly555del
ENST00000503569.5:c.1663_1665del	ENSP00000423337.1:p.Gly555del
ENST00000507765.1:n.1848_1850del
NM_001145853.1:c.1663_1665del	NP_001139325.1:p.Gly555del
NM_006005.3:c.1663_1665del MANE Select	NP_005996.2:p.Gly555del
XM_017008586.1:c.1672_1674del	XP_016864075.1:p.Gly558del