Canonical Allele Identifier: CA463585732

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558628T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558628T>C , CM000671.2:g.6558628T>C	GRCh38
NC_000009.11:g.6558628T>C , CM000671.1:g.6558628T>C	GRCh37
NC_000009.10:g.6548628T>C	NCBI36
NG_016397.1:g.92065A>G , LRG_643:g.92065A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1983A>G MANE Select	ENSP00000370737.4:p.Ala661=
ENST00000460457.2:n.143A>G
ENST00000638233.1:n.418A>G
ENST00000638661.1:c.183A>G	ENSP00000491369.1:p.Ala61=
ENST00000638694.1:n.170A>G
ENST00000639318.1:c.183A>G	ENSP00000491932.1:p.Ala61=
ENST00000639364.1:n.1683A>G
ENST00000639443.1:n.1551A>G
ENST00000639954.1:n.1691A>G
ENST00000640208.1:c.183A>G	ENSP00000491895.1:p.Ala61=
ENST00000640505.1:n.222A>G
ENST00000640592.1:n.1866A>G
ENST00000321612.6:c.1983A>G	ENSP00000370737.3:p.Ala661=
ENST00000460457.1:n.122A>G
NM_000170.2:c.1983A>G , LRG_643t1:c.1983A>G	NP_000161.2:p.Ala661=
NM_000170.3:c.1983A>G MANE Select	NP_000161.2:p.Ala661=