Canonical Allele Identifier: CA188649114

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6550898C>T , CM000671.2:g.6550898C>T	GRCh38
NC_000009.11:g.6550898C>T , CM000671.1:g.6550898C>T	GRCh37
NC_000009.10:g.6540898C>T	NCBI36
NG_016397.1:g.99795G>A , LRG_643:g.99795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2474G>A MANE Select	ENSP00000370737.4:p.Gly825Asp
ENST00000638233.1:n.909G>A
ENST00000638661.1:c.674G>A	ENSP00000491369.1:p.Gly225Asp
ENST00000638694.1:n.661G>A
ENST00000639318.1:c.674G>A	ENSP00000491932.1:p.Gly225Asp
ENST00000639364.1:n.2174G>A
ENST00000639443.1:n.2042G>A
ENST00000639639.1:c.176G>A	ENSP00000491312.1:p.Gly59Asp
ENST00000639954.1:n.2182G>A
ENST00000640505.1:n.713G>A
ENST00000321612.6:c.2474G>A	ENSP00000370737.3:p.Gly825Asp
NM_000170.2:c.2474G>A , LRG_643t1:c.2474G>A	NP_000161.2:p.Gly825Asp
NM_000170.3:c.2474G>A MANE Select	NP_000161.2:p.Gly825Asp