Canonical Allele Identifier: CA1830503819
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6565364C= , CM000671.2:g.6565364C= GRCh38
NC_000009.11:g.6565364C= , CM000671.1:g.6565364C= GRCh37
NC_000009.10:g.6555364C= NCBI36
NG_016397.1:g.85329G= , LRG_643:g.85329G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1916G= MANE Select ENSP00000370737.4:p.Gly639=
ENST00000460457.2:n.76G=
ENST00000638233.1:n.351G=
ENST00000638661.1:c.116G= ENSP00000491369.1:p.Gly39=
ENST00000638694.1:n.103G=
ENST00000639318.1:c.116G= ENSP00000491932.1:p.Gly39=
ENST00000639364.1:n.1616G=
ENST00000639443.1:n.1484G=
ENST00000639954.1:n.1624G=
ENST00000640208.1:c.116G= ENSP00000491895.1:p.Gly39=
ENST00000640505.1:n.155G=
ENST00000640592.1:n.1799G=
ENST00000321612.6:c.1916G= ENSP00000370737.3:p.Gly639=
ENST00000460457.1:n.55G=
NM_000170.2:c.1916G= , LRG_643t1:c.1916G= NP_000161.2:p.Gly639=
NM_000170.3:c.1916G= MANE Select NP_000161.2:p.Gly639=