Canonical Allele Identifier: CA2669843460

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301732-TCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301736_6301738del , CM000666.2:g.6301736_6301738del	GRCh38
NC_000004.11:g.6303463_6303465del , CM000666.1:g.6303463_6303465del	GRCh37
NC_000004.10:g.6354364_6354366del	NCBI36
NG_011700.1:g.36887_36889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1977_1979del	ENSP00000507852.1:p.Cys659del
ENST00000683395.1:c.1918_1920del
ENST00000684087.1:c.1941_1943del	ENSP00000506978.1:p.Cys647del
ENST00000506362.2:c.1692_1694del	ENSP00000424103.2:p.Cys564del
ENST00000673642.1:c.1600_1602del	ENSP00000501242.1:n.1600_1602del
ENST00000673991.1:c.1977_1979del	ENSP00000501033.1:p.Cys659del
ENST00000226760.5:c.1941_1943del MANE Select	ENSP00000226760.1:p.Cys647del
ENST00000503569.5:c.1941_1943del	ENSP00000423337.1:p.Cys647del
ENST00000507765.1:n.2126_2128del
NM_001145853.1:c.1941_1943del	NP_001139325.1:p.Cys647del
NM_006005.3:c.1941_1943del MANE Select	NP_005996.2:p.Cys647del
XM_017008586.1:c.1950_1952del	XP_016864075.1:p.Cys650del