Canonical Allele Identifier: CA1435768943

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291918_6291919delinsTG , CM000666.2:g.6291918_6291919delinsTG	GRCh38
NC_000004.11:g.6293645_6293646delinsTG , CM000666.1:g.6293645_6293646delinsTG	GRCh37
NC_000004.10:g.6344546_6344547delinsTG	NCBI36
NG_011700.1:g.27069_27070delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.633_634delinsTG	ENSP00000507852.1:p.Asp211=
ENST00000683395.1:c.610_611delinsTG
ENST00000684087.1:c.633_634delinsTG	ENSP00000506978.1:p.Asp211=
ENST00000506362.2:c.384_385delinsTG	ENSP00000424103.2:p.Asp128=
ENST00000673642.1:c.432_433delinsTG	ENSP00000501242.1:p.Asp144=
ENST00000673991.1:c.633_634delinsTG	ENSP00000501033.1:p.Asp211=
ENST00000226760.5:c.633_634delinsTG MANE Select	ENSP00000226760.1:p.Asp211=
ENST00000503569.5:c.633_634delinsTG	ENSP00000423337.1:p.Asp211=
ENST00000506362.1:c.230_231delinsTG
ENST00000507765.1:n.818_819delinsTG
NM_001145853.1:c.633_634delinsTG	NP_001139325.1:p.Asp211=
NM_006005.3:c.633_634delinsTG MANE Select	NP_005996.2:p.Asp211=
XM_017008586.1:c.642_643delinsTG	XP_016864075.1:p.Asp214=