Canonical Allele Identifier: CA1830496352
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558601C= , CM000671.2:g.6558601C= GRCh38
NC_000009.11:g.6558601C= , CM000671.1:g.6558601C= GRCh37
NC_000009.10:g.6548601C= NCBI36
NG_016397.1:g.92092G= , LRG_643:g.92092G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2010G= MANE Select ENSP00000370737.4:p.Val670=
ENST00000460457.2:n.170G=
ENST00000638233.1:n.445G=
ENST00000638661.1:c.210G= ENSP00000491369.1:p.Val70=
ENST00000638694.1:n.197G=
ENST00000639318.1:c.210G= ENSP00000491932.1:p.Val70=
ENST00000639364.1:n.1710G=
ENST00000639443.1:n.1578G=
ENST00000639954.1:n.1718G=
ENST00000640208.1:c.210G= ENSP00000491895.1:p.Val70=
ENST00000640505.1:n.249G=
ENST00000640592.1:n.1893G=
ENST00000321612.6:c.2010G= ENSP00000370737.3:p.Val670=
ENST00000460457.1:n.149G=
NM_000170.2:c.2010G= , LRG_643t1:c.2010G= NP_000161.2:p.Val670=
NM_000170.3:c.2010G= MANE Select NP_000161.2:p.Val670=