Canonical Allele Identifier: CA463585537

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556231C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556231C>T , CM000671.2:g.6556231C>T	GRCh38
NC_000009.11:g.6556231C>T , CM000671.1:g.6556231C>T	GRCh37
NC_000009.10:g.6546231C>T	NCBI36
NG_016397.1:g.94462G>A , LRG_643:g.94462G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2124G>A MANE Select	ENSP00000370737.4:p.Glu708=
ENST00000638233.1:n.559G>A
ENST00000638661.1:c.324G>A	ENSP00000491369.1:p.Glu108=
ENST00000638694.1:n.311G>A
ENST00000639318.1:c.324G>A	ENSP00000491932.1:p.Glu108=
ENST00000639364.1:n.1824G>A
ENST00000639443.1:n.1692G>A
ENST00000639954.1:n.1832G>A
ENST00000640505.1:n.363G>A
ENST00000321612.6:c.2124G>A	ENSP00000370737.3:p.Glu708=
NM_000170.2:c.2124G>A , LRG_643t1:c.2124G>A	NP_000161.2:p.Glu708=
NM_000170.3:c.2124G>A MANE Select	NP_000161.2:p.Glu708=