Canonical Allele Identifier: CA372881278

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556210G>T (hg19) ; chr9:g.6556210G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556210G>T , CM000671.2:g.6556210G>T	GRCh38
NC_000009.11:g.6556210G>T , CM000671.1:g.6556210G>T	GRCh37
NC_000009.10:g.6546210G>T	NCBI36
NG_016397.1:g.94483C>A , LRG_643:g.94483C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2145C>A MANE Select	ENSP00000370737.4:p.Asp715Glu
ENST00000638233.1:n.580C>A
ENST00000638661.1:c.345C>A	ENSP00000491369.1:p.Asp115Glu
ENST00000638694.1:n.332C>A
ENST00000639318.1:c.345C>A	ENSP00000491932.1:p.Asp115Glu
ENST00000639364.1:n.1845C>A
ENST00000639443.1:n.1713C>A
ENST00000639954.1:n.1853C>A
ENST00000640505.1:n.384C>A
ENST00000321612.6:c.2145C>A	ENSP00000370737.3:p.Asp715Glu
NM_000170.2:c.2145C>A , LRG_643t1:c.2145C>A	NP_000161.2:p.Asp715Glu
NM_000170.3:c.2145C>A MANE Select	NP_000161.2:p.Asp715Glu