Canonical Allele Identifier: CA372882079

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558656C>G (hg19) ; chr9:g.6558656C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558656C>G , CM000671.2:g.6558656C>G	GRCh38
NC_000009.11:g.6558656C>G , CM000671.1:g.6558656C>G	GRCh37
NC_000009.10:g.6548656C>G	NCBI36
NG_016397.1:g.92037G>C , LRG_643:g.92037G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1955G>C MANE Select	ENSP00000370737.4:p.Gly652Ala
ENST00000460457.2:n.115G>C
ENST00000638233.1:n.390G>C
ENST00000638661.1:c.155G>C	ENSP00000491369.1:p.Gly52Ala
ENST00000638694.1:n.142G>C
ENST00000639318.1:c.155G>C	ENSP00000491932.1:p.Gly52Ala
ENST00000639364.1:n.1655G>C
ENST00000639443.1:n.1523G>C
ENST00000639954.1:n.1663G>C
ENST00000640208.1:c.155G>C	ENSP00000491895.1:p.Gly52Ala
ENST00000640505.1:n.194G>C
ENST00000640592.1:n.1838G>C
ENST00000321612.6:c.1955G>C	ENSP00000370737.3:p.Gly652Ala
ENST00000460457.1:n.94G>C
NM_000170.2:c.1955G>C , LRG_643t1:c.1955G>C	NP_000161.2:p.Gly652Ala
NM_000170.3:c.1955G>C MANE Select	NP_000161.2:p.Gly652Ala