Canonical Allele Identifier: CA372881811

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558563G>T (hg19) ; chr9:g.6558563G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558563G>T , CM000671.2:g.6558563G>T	GRCh38
NC_000009.11:g.6558563G>T , CM000671.1:g.6558563G>T	GRCh37
NC_000009.10:g.6548563G>T	NCBI36
NG_016397.1:g.92130C>A , LRG_643:g.92130C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2048C>A MANE Select	ENSP00000370737.4:p.Ala683Asp
ENST00000460457.2:n.208C>A
ENST00000638233.1:n.483C>A
ENST00000638661.1:c.248C>A	ENSP00000491369.1:p.Ala83Asp
ENST00000638694.1:n.235C>A
ENST00000639318.1:c.248C>A	ENSP00000491932.1:p.Ala83Asp
ENST00000639364.1:n.1748C>A
ENST00000639443.1:n.1616C>A
ENST00000639954.1:n.1756C>A
ENST00000640208.1:c.248C>A	ENSP00000491895.1:p.Ala83Asp
ENST00000640505.1:n.287C>A
ENST00000640592.1:n.1931C>A
ENST00000321612.6:c.2048C>A	ENSP00000370737.3:p.Ala683Asp
ENST00000460457.1:n.187C>A
NM_000170.2:c.2048C>A , LRG_643t1:c.2048C>A	NP_000161.2:p.Ala683Asp
NM_000170.3:c.2048C>A MANE Select	NP_000161.2:p.Ala683Asp