Canonical Allele Identifier: CA1435771733

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301725_6301733delinsGTGCTGTTC , CM000666.2:g.6301725_6301733delinsGTGCTGTTC	GRCh38
NC_000004.11:g.6303452_6303460delinsGTGCTGTTC , CM000666.1:g.6303452_6303460delinsGTGCTGTTC	GRCh37
NC_000004.10:g.6354353_6354361delinsGTGCTGTTC	NCBI36
NG_011700.1:g.36876_36884delinsGTGCTGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1966_1974delinsGTGCTGTTC	ENSP00000507852.1:p.Val656=
ENST00000683395.1:c.1907_1915delinsGTGCTGTTC
ENST00000684087.1:c.1930_1938delinsGTGCTGTTC	ENSP00000506978.1:p.Val644=
ENST00000506362.2:c.1681_1689delinsGTGCTGTTC	ENSP00000424103.2:p.Val561=
ENST00000673642.1:c.1589_1597delinsGTGCTGTTC	ENSP00000501242.1:n.1589_1597delinsGTGCTGTTC
ENST00000673991.1:c.1966_1974delinsGTGCTGTTC	ENSP00000501033.1:p.Val656=
ENST00000226760.5:c.1930_1938delinsGTGCTGTTC MANE Select	ENSP00000226760.1:p.Val644=
ENST00000503569.5:c.1930_1938delinsGTGCTGTTC	ENSP00000423337.1:p.Val644=
ENST00000507765.1:n.2115_2123delinsGTGCTGTTC
NM_001145853.1:c.1930_1938delinsGTGCTGTTC	NP_001139325.1:p.Val644=
NM_006005.3:c.1930_1938delinsGTGCTGTTC MANE Select	NP_005996.2:p.Val644=
XM_017008586.1:c.1939_1947delinsGTGCTGTTC	XP_016864075.1:p.Val647=