Canonical Allele Identifier: CA1058891853
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1385982223

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301519_6301536dup , CM000666.2:g.6301519_6301536dup GRCh38
NC_000004.11:g.6303246_6303263dup , CM000666.1:g.6303246_6303263dup GRCh37
NC_000004.10:g.6354147_6354164dup NCBI36
NG_011700.1:g.36670_36687dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1760_1777dup ENSP00000507852.1:p.Val592_Gly593insAlaGl...
ENST00000683395.1:c.1701_1718dup
ENST00000684087.1:c.1724_1741dup ENSP00000506978.1:p.Val580_Gly581insAlaGl...
ENST00000506362.2:c.1475_1492dup ENSP00000424103.2:p.Val497_Gly498insAlaGl...
ENST00000673642.1:c.1383_1400dup ENSP00000501242.1:n.1383_1400dup
ENST00000673991.1:c.1760_1777dup ENSP00000501033.1:p.Val592_Gly593insAlaGl...
ENST00000226760.5:c.1724_1741dup MANE Select ENSP00000226760.1:p.Val580_Gly581insAlaGl...
ENST00000503569.5:c.1724_1741dup ENSP00000423337.1:p.Val580_Gly581insAlaGl...
ENST00000507765.1:n.1909_1926dup
NM_001145853.1:c.1724_1741dup NP_001139325.1:p.Val580_Gly581insAlaGlyLe...
NM_006005.3:c.1724_1741dup MANE Select NP_005996.2:p.Val580_Gly581insAlaGlyLeuAl...
XM_017008586.1:c.1733_1750dup XP_016864075.1:p.Val583_Gly584insAlaGlyLe...