Canonical Allele Identifier: CA463585573

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556300C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556300C>G , CM000671.2:g.6556300C>G	GRCh38
NC_000009.11:g.6556300C>G , CM000671.1:g.6556300C>G	GRCh37
NC_000009.10:g.6546300C>G	NCBI36
NG_016397.1:g.94393G>C , LRG_643:g.94393G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2055G>C MANE Select	ENSP00000370737.4:p.Val685=
ENST00000638233.1:n.490G>C
ENST00000638661.1:c.255G>C	ENSP00000491369.1:p.Val85=
ENST00000638694.1:n.242G>C
ENST00000639318.1:c.255G>C	ENSP00000491932.1:p.Val85=
ENST00000639364.1:n.1755G>C
ENST00000639443.1:n.1623G>C
ENST00000639954.1:n.1763G>C
ENST00000640505.1:n.294G>C
ENST00000321612.6:c.2055G>C	ENSP00000370737.3:p.Val685=
NM_000170.2:c.2055G>C , LRG_643t1:c.2055G>C	NP_000161.2:p.Val685=
NM_000170.3:c.2055G>C MANE Select	NP_000161.2:p.Val685=