Canonical Allele Identifier: CA1830496368
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558606C= , CM000671.2:g.6558606C= GRCh38
NC_000009.11:g.6558606C= , CM000671.1:g.6558606C= GRCh37
NC_000009.10:g.6548606C= NCBI36
NG_016397.1:g.92087G= , LRG_643:g.92087G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2005G= MANE Select ENSP00000370737.4:p.Glu669=
ENST00000460457.2:n.165G=
ENST00000638233.1:n.440G=
ENST00000638661.1:c.205G= ENSP00000491369.1:p.Glu69=
ENST00000638694.1:n.192G=
ENST00000639318.1:c.205G= ENSP00000491932.1:p.Glu69=
ENST00000639364.1:n.1705G=
ENST00000639443.1:n.1573G=
ENST00000639954.1:n.1713G=
ENST00000640208.1:c.205G= ENSP00000491895.1:p.Glu69=
ENST00000640505.1:n.244G=
ENST00000640592.1:n.1888G=
ENST00000321612.6:c.2005G= ENSP00000370737.3:p.Glu669=
ENST00000460457.1:n.144G=
NM_000170.2:c.2005G= , LRG_643t1:c.2005G= NP_000161.2:p.Glu669=
NM_000170.3:c.2005G= MANE Select NP_000161.2:p.Glu669=