Canonical Allele Identifier: CA372879991

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6554673C>G (hg19) ; chr9:g.6554673C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6554673C>G , CM000671.2:g.6554673C>G	GRCh38
NC_000009.11:g.6554673C>G , CM000671.1:g.6554673C>G	GRCh37
NC_000009.10:g.6544673C>G	NCBI36
NG_016397.1:g.96020G>C , LRG_643:g.96020G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2311G>C MANE Select	ENSP00000370737.4:p.Gly771Arg
ENST00000638233.1:n.746G>C
ENST00000638661.1:c.511G>C	ENSP00000491369.1:p.Gly171Arg
ENST00000638694.1:n.498G>C
ENST00000639318.1:c.511G>C	ENSP00000491932.1:p.Gly171Arg
ENST00000639364.1:n.2011G>C
ENST00000639443.1:n.1879G>C
ENST00000639639.1:c.13G>C	ENSP00000491312.1:p.Gly5Arg
ENST00000639954.1:n.2019G>C
ENST00000640505.1:n.550G>C
ENST00000321612.6:c.2311G>C	ENSP00000370737.3:p.Gly771Arg
ENST00000467946.1:n.237G>C
NM_000170.2:c.2311G>C , LRG_643t1:c.2311G>C	NP_000161.2:p.Gly771Arg
NM_000170.3:c.2311G>C MANE Select	NP_000161.2:p.Gly771Arg