Canonical Allele Identifier: CA463585558

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556273A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556273A>C , CM000671.2:g.6556273A>C	GRCh38
NC_000009.11:g.6556273A>C , CM000671.1:g.6556273A>C	GRCh37
NC_000009.10:g.6546273A>C	NCBI36
NG_016397.1:g.94420T>G , LRG_643:g.94420T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2082T>G MANE Select	ENSP00000370737.4:p.Ala694=
ENST00000638233.1:n.517T>G
ENST00000638661.1:c.282T>G	ENSP00000491369.1:p.Ala94=
ENST00000638694.1:n.269T>G
ENST00000639318.1:c.282T>G	ENSP00000491932.1:p.Ala94=
ENST00000639364.1:n.1782T>G
ENST00000639443.1:n.1650T>G
ENST00000639954.1:n.1790T>G
ENST00000640505.1:n.321T>G
ENST00000321612.6:c.2082T>G	ENSP00000370737.3:p.Ala694=
NM_000170.2:c.2082T>G , LRG_643t1:c.2082T>G	NP_000161.2:p.Ala694=
NM_000170.3:c.2082T>G MANE Select	NP_000161.2:p.Ala694=