Canonical Allele Identifier: CA372881274
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 1994478
ClinVar RCV Id: RCV002791168

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556209G>A , CM000671.2:g.6556209G>A GRCh38
NC_000009.11:g.6556209G>A , CM000671.1:g.6556209G>A GRCh37
NC_000009.10:g.6546209G>A NCBI36
NG_016397.1:g.94484C>T , LRG_643:g.94484C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.2146C>T MANE Select ENSP00000370737.4:p.Leu716Phe
ENST00000638233.1:n.581C>T
ENST00000638661.1:c.346C>T ENSP00000491369.1:p.Leu116Phe
ENST00000638694.1:n.333C>T
ENST00000639318.1:c.346C>T ENSP00000491932.1:p.Leu116Phe
ENST00000639364.1:n.1846C>T
ENST00000639443.1:n.1714C>T
ENST00000639954.1:n.1854C>T
ENST00000640505.1:n.385C>T
ENST00000321612.6:c.2146C>T ENSP00000370737.3:p.Leu716Phe
NM_000170.2:c.2146C>T , LRG_643t1:c.2146C>T NP_000161.2:p.Leu716Phe
NM_000170.3:c.2146C>T MANE Select NP_000161.2:p.Leu716Phe