Canonical Allele Identifier: CA1830527767
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6595031G= , CM000671.2:g.6595031G= GRCh38
NC_000009.11:g.6595031G= , CM000671.1:g.6595031G= GRCh37
NC_000009.10:g.6585031G= NCBI36
NG_016397.1:g.55662C= , LRG_643:g.55662C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1244C= MANE Select ENSP00000370737.4:p.Thr415=
ENST00000638654.1:c.491C= ENSP00000491101.1:p.Thr164=
ENST00000639364.1:n.944C=
ENST00000639443.1:n.812C=
ENST00000639493.1:n.396C=
ENST00000639954.1:n.952C=
ENST00000640592.1:n.1127C=
ENST00000321612.6:c.1244C= ENSP00000370737.3:p.Thr415=
ENST00000463305.1:n.328C=
NM_000170.2:c.1244C= , LRG_643t1:c.1244C= NP_000161.2:p.Thr415=
NM_000170.3:c.1244C= MANE Select NP_000161.2:p.Thr415=