Canonical Allele Identifier: CA2586973630
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301384_6301387dup , CM000666.2:g.6301384_6301387dup GRCh38
NC_000004.11:g.6303111_6303114dup , CM000666.1:g.6303111_6303114dup GRCh37
NC_000004.10:g.6354012_6354015dup NCBI36
NG_011700.1:g.36535_36538dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1625_1628dup ENSP00000507852.1:p.Val544ProfsTer12
ENST00000683395.1:c.1566_1569dup
ENST00000684087.1:c.1589_1592dup ENSP00000506978.1:p.Val532ProfsTer12
ENST00000506362.2:c.1340_1343dup ENSP00000424103.2:p.Val449ProfsTer12
ENST00000673642.1:c.1248_1251dup ENSP00000501242.1:p.Cys418ThrfsTer?
ENST00000673991.1:c.1625_1628dup ENSP00000501033.1:p.Val544ProfsTer12
ENST00000226760.5:c.1589_1592dup MANE Select ENSP00000226760.1:p.Val532ProfsTer12
ENST00000503569.5:c.1589_1592dup ENSP00000423337.1:p.Val532ProfsTer12
ENST00000507765.1:n.1774_1777dup
NM_001145853.1:c.1589_1592dup NP_001139325.1:p.Val532ProfsTer12
NM_006005.3:c.1589_1592dup MANE Select NP_005996.2:p.Val532ProfsTer12
XM_017008586.1:c.1598_1601dup XP_016864075.1:p.Val535ProfsTer12