Canonical Allele Identifier: CA1830493519
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556227T= , CM000671.2:g.6556227T= GRCh38
NC_000009.11:g.6556227T= , CM000671.1:g.6556227T= GRCh37
NC_000009.10:g.6546227T= NCBI36
NG_016397.1:g.94466A= , LRG_643:g.94466A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2128A= MANE Select ENSP00000370737.4:p.Ile710=
ENST00000638233.1:n.563A=
ENST00000638661.1:c.328A= ENSP00000491369.1:p.Ile110=
ENST00000638694.1:n.315A=
ENST00000639318.1:c.328A= ENSP00000491932.1:p.Ile110=
ENST00000639364.1:n.1828A=
ENST00000639443.1:n.1696A=
ENST00000639954.1:n.1836A=
ENST00000640505.1:n.367A=
ENST00000321612.6:c.2128A= ENSP00000370737.3:p.Ile710=
NM_000170.2:c.2128A= , LRG_643t1:c.2128A= NP_000161.2:p.Ile710=
NM_000170.3:c.2128A= MANE Select NP_000161.2:p.Ile710=