Canonical Allele Identifier: CA1830493660
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556285C= , CM000671.2:g.6556285C= GRCh38
NC_000009.11:g.6556285C= , CM000671.1:g.6556285C= GRCh37
NC_000009.10:g.6546285C= NCBI36
NG_016397.1:g.94408G= , LRG_643:g.94408G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2070G= MANE Select ENSP00000370737.4:p.Glu690=
ENST00000638233.1:n.505G=
ENST00000638661.1:c.270G= ENSP00000491369.1:p.Glu90=
ENST00000638694.1:n.257G=
ENST00000639318.1:c.270G= ENSP00000491932.1:p.Glu90=
ENST00000639364.1:n.1770G=
ENST00000639443.1:n.1638G=
ENST00000639954.1:n.1778G=
ENST00000640505.1:n.309G=
ENST00000321612.6:c.2070G= ENSP00000370737.3:p.Glu690=
NM_000170.2:c.2070G= , LRG_643t1:c.2070G= NP_000161.2:p.Glu690=
NM_000170.3:c.2070G= MANE Select NP_000161.2:p.Glu690=