Canonical Allele Identifier: CA1830496257
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558563G= , CM000671.2:g.6558563G= GRCh38
NC_000009.11:g.6558563G= , CM000671.1:g.6558563G= GRCh37
NC_000009.10:g.6548563G= NCBI36
NG_016397.1:g.92130C= , LRG_643:g.92130C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2048C= MANE Select ENSP00000370737.4:p.Ala683=
ENST00000460457.2:n.208C=
ENST00000638233.1:n.483C=
ENST00000638661.1:c.248C= ENSP00000491369.1:p.Ala83=
ENST00000638694.1:n.235C=
ENST00000639318.1:c.248C= ENSP00000491932.1:p.Ala83=
ENST00000639364.1:n.1748C=
ENST00000639443.1:n.1616C=
ENST00000639954.1:n.1756C=
ENST00000640208.1:c.248C= ENSP00000491895.1:p.Ala83=
ENST00000640505.1:n.287C=
ENST00000640592.1:n.1931C=
ENST00000321612.6:c.2048C= ENSP00000370737.3:p.Ala683=
ENST00000460457.1:n.187C=
NM_000170.2:c.2048C= , LRG_643t1:c.2048C= NP_000161.2:p.Ala683=
NM_000170.3:c.2048C= MANE Select NP_000161.2:p.Ala683=