Canonical Allele Identifier: CA1830493610
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556262G= , CM000671.2:g.6556262G= GRCh38
NC_000009.11:g.6556262G= , CM000671.1:g.6556262G= GRCh37
NC_000009.10:g.6546262G= NCBI36
NG_016397.1:g.94431C= , LRG_643:g.94431C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2093C= MANE Select ENSP00000370737.4:p.Thr698=
ENST00000638233.1:n.528C=
ENST00000638661.1:c.293C= ENSP00000491369.1:p.Thr98=
ENST00000638694.1:n.280C=
ENST00000639318.1:c.293C= ENSP00000491932.1:p.Thr98=
ENST00000639364.1:n.1793C=
ENST00000639443.1:n.1661C=
ENST00000639954.1:n.1801C=
ENST00000640505.1:n.332C=
ENST00000321612.6:c.2093C= ENSP00000370737.3:p.Thr698=
NM_000170.2:c.2093C= , LRG_643t1:c.2093C= NP_000161.2:p.Thr698=
NM_000170.3:c.2093C= MANE Select NP_000161.2:p.Thr698=