Canonical Allele Identifier: CA1830493396
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556191C= , CM000671.2:g.6556191C= GRCh38
NC_000009.11:g.6556191C= , CM000671.1:g.6556191C= GRCh37
NC_000009.10:g.6546191C= NCBI36
NG_016397.1:g.94502G= , LRG_643:g.94502G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2164G= MANE Select ENSP00000370737.4:p.Gly722=
ENST00000638233.1:n.599G=
ENST00000638661.1:c.364G= ENSP00000491369.1:p.Gly122=
ENST00000638694.1:n.351G=
ENST00000639318.1:c.364G= ENSP00000491932.1:p.Gly122=
ENST00000639364.1:n.1864G=
ENST00000639443.1:n.1732G=
ENST00000639954.1:n.1872G=
ENST00000640505.1:n.403G=
ENST00000321612.6:c.2164G= ENSP00000370737.3:p.Gly722=
NM_000170.2:c.2164G= , LRG_643t1:c.2164G= NP_000161.2:p.Gly722=
NM_000170.3:c.2164G= MANE Select NP_000161.2:p.Gly722=