Canonical Allele Identifier: CA438368532
Gene: WFS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.6303073C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301346C>G , CM000666.2:g.6301346C>G GRCh38
NC_000004.11:g.6303073C>G , CM000666.1:g.6303073C>G GRCh37
NC_000004.10:g.6353974C>G NCBI36
NG_011700.1:g.36497C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1587C>G ENSP00000507852.1:p.Arg529=
ENST00000683395.1:c.1528C>G
ENST00000684087.1:c.1551C>G ENSP00000506978.1:p.Arg517=
ENST00000506362.2:c.1302C>G ENSP00000424103.2:p.Arg434=
ENST00000673642.1:c.1210C>G ENSP00000501242.1:p.His404Asp
ENST00000673991.1:c.1587C>G ENSP00000501033.1:p.Arg529=
ENST00000226760.5:c.1551C>G MANE Select ENSP00000226760.1:p.Arg517=
ENST00000503569.5:c.1551C>G ENSP00000423337.1:p.Arg517=
ENST00000507765.1:n.1736C>G
NM_001145853.1:c.1551C>G NP_001139325.1:p.Arg517=
NM_006005.3:c.1551C>G MANE Select NP_005996.2:p.Arg517=
XM_017008586.1:c.1560C>G XP_016864075.1:p.Arg520=