Canonical Allele Identifier: CA372881942

Gene: GLDC

Linked Data

• dbSNP Id: rs1817684504
• MyVariant Identifiers: chr9:g.6558626C>G (hg19) ; chr9:g.6558626C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558626C>G , CM000671.2:g.6558626C>G	GRCh38
NC_000009.11:g.6558626C>G , CM000671.1:g.6558626C>G	GRCh37
NC_000009.10:g.6548626C>G	NCBI36
NG_016397.1:g.92067G>C , LRG_643:g.92067G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1985G>C MANE Select	ENSP00000370737.4:p.Gly662Ala
ENST00000460457.2:n.145G>C
ENST00000638233.1:n.420G>C
ENST00000638661.1:c.185G>C	ENSP00000491369.1:p.Gly62Ala
ENST00000638694.1:n.172G>C
ENST00000639318.1:c.185G>C	ENSP00000491932.1:p.Gly62Ala
ENST00000639364.1:n.1685G>C
ENST00000639443.1:n.1553G>C
ENST00000639954.1:n.1693G>C
ENST00000640208.1:c.185G>C	ENSP00000491895.1:p.Gly62Ala
ENST00000640505.1:n.224G>C
ENST00000640592.1:n.1868G>C
ENST00000321612.6:c.1985G>C	ENSP00000370737.3:p.Gly662Ala
ENST00000460457.1:n.124G>C
NM_000170.2:c.1985G>C , LRG_643t1:c.1985G>C	NP_000161.2:p.Gly662Ala
NM_000170.3:c.1985G>C MANE Select	NP_000161.2:p.Gly662Ala