Canonical Allele Identifier: CA1435774275

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301624_6301640delinsTGCGCTGGTGGACCAAG , CM000666.2:g.6301624_6301640delinsTGCGCTGGTGGACCAAG	GRCh38
NC_000004.11:g.6303351_6303367delinsTGCGCTGGTGGACCAAG , CM000666.1:g.6303351_6303367delinsTGCGCTGGTGGACCAAG	GRCh37
NC_000004.10:g.6354252_6354268delinsTGCGCTGGTGGACCAAG	NCBI36
NG_011700.1:g.36775_36791delinsTGCGCTGGTGGACCAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.1865_1881delinsTGCGCTGGTGGACCAAG	ENSP00000507852.1:p.Leu622=
ENST00000683395.1:c.1806_1822delinsTGCGCTGGTGGACCAAG
ENST00000684087.1:c.1829_1845delinsTGCGCTGGTGGACCAAG	ENSP00000506978.1:p.Leu610=
ENST00000506362.2:c.1580_1596delinsTGCGCTGGTGGACCAAG	ENSP00000424103.2:p.Leu527=
ENST00000673642.1:c.1488_1504delinsTGCGCTGGTGGACCAAG	ENSP00000501242.1:n.1488_1504delinsTGCGCT...
ENST00000673991.1:c.1865_1881delinsTGCGCTGGTGGACCAAG	ENSP00000501033.1:p.Leu622=
ENST00000226760.5:c.1829_1845delinsTGCGCTGGTGGACCAAG MANE Select	ENSP00000226760.1:p.Leu610=
ENST00000503569.5:c.1829_1845delinsTGCGCTGGTGGACCAAG	ENSP00000423337.1:p.Leu610=
ENST00000507765.1:n.2014_2030delinsTGCGCTGGTGGACCAAG
NM_001145853.1:c.1829_1845delinsTGCGCTGGTGGACCAAG	NP_001139325.1:p.Leu610=
NM_006005.3:c.1829_1845delinsTGCGCTGGTGGACCAAG MANE Select	NP_005996.2:p.Leu610=
XM_017008586.1:c.1838_1854delinsTGCGCTGGTGGACCAAG	XP_016864075.1:p.Leu613=