Canonical Allele Identifier: CA2669843446
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301463_6301464insGAGTC , CM000666.2:g.6301463_6301464insGAGTC GRCh38
NC_000004.11:g.6303190_6303191insGAGTC , CM000666.1:g.6303190_6303191insGAGTC GRCh37
NC_000004.10:g.6354091_6354092insGAGTC NCBI36
NG_011700.1:g.36614_36615insGAGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1704_1705insGAGTC ENSP00000507852.1:p.Leu569GlufsTer?
ENST00000683395.1:c.1645_1646insGAGTC
ENST00000684087.1:c.1668_1669insGAGTC ENSP00000506978.1:p.Leu557GlufsTer?
ENST00000506362.2:c.1419_1420insGAGTC ENSP00000424103.2:p.Leu474GlufsTer?
ENST00000673642.1:c.1327_1328insGAGTC ENSP00000501242.1:n.1327_1328insGAGTC
ENST00000673991.1:c.1704_1705insGAGTC ENSP00000501033.1:p.Leu569GlufsTer?
ENST00000226760.5:c.1668_1669insGAGTC MANE Select ENSP00000226760.1:p.Leu557GlufsTer?
ENST00000503569.5:c.1668_1669insGAGTC ENSP00000423337.1:p.Leu557GlufsTer?
ENST00000507765.1:n.1853_1854insGAGTC
NM_001145853.1:c.1668_1669insGAGTC NP_001139325.1:p.Leu557GlufsTer?
NM_006005.3:c.1668_1669insGAGTC MANE Select NP_005996.2:p.Leu557GlufsTer?
XM_017008586.1:c.1677_1678insGAGTC XP_016864075.1:p.Leu560GlufsTer?