Canonical Allele Identifier: CA1830493389
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556189T= , CM000671.2:g.6556189T= GRCh38
NC_000009.11:g.6556189T= , CM000671.1:g.6556189T= GRCh37
NC_000009.10:g.6546189T= NCBI36
NG_016397.1:g.94504A= , LRG_643:g.94504A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2166A= MANE Select ENSP00000370737.4:p.Gly722=
ENST00000638233.1:n.601A=
ENST00000638661.1:c.366A= ENSP00000491369.1:p.Gly122=
ENST00000638694.1:n.353A=
ENST00000639318.1:c.366A= ENSP00000491932.1:p.Gly122=
ENST00000639364.1:n.1866A=
ENST00000639443.1:n.1734A=
ENST00000639954.1:n.1874A=
ENST00000640505.1:n.405A=
ENST00000321612.6:c.2166A= ENSP00000370737.3:p.Gly722=
NM_000170.2:c.2166A= , LRG_643t1:c.2166A= NP_000161.2:p.Gly722=
NM_000170.3:c.2166A= MANE Select NP_000161.2:p.Gly722=