Canonical Allele Identifier: CA463585846

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558661T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558661T>G , CM000671.2:g.6558661T>G	GRCh38
NC_000009.11:g.6558661T>G , CM000671.1:g.6558661T>G	GRCh37
NC_000009.10:g.6548661T>G	NCBI36
NG_016397.1:g.92032A>C , LRG_643:g.92032A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1950A>C MANE Select	ENSP00000370737.4:p.Ala650=
ENST00000460457.2:n.110A>C
ENST00000638233.1:n.385A>C
ENST00000638661.1:c.150A>C	ENSP00000491369.1:p.Ala50=
ENST00000638694.1:n.137A>C
ENST00000639318.1:c.150A>C	ENSP00000491932.1:p.Ala50=
ENST00000639364.1:n.1650A>C
ENST00000639443.1:n.1518A>C
ENST00000639954.1:n.1658A>C
ENST00000640208.1:c.150A>C	ENSP00000491895.1:p.Ala50=
ENST00000640505.1:n.189A>C
ENST00000640592.1:n.1833A>C
ENST00000321612.6:c.1950A>C	ENSP00000370737.3:p.Ala650=
ENST00000460457.1:n.89A>C
NM_000170.2:c.1950A>C , LRG_643t1:c.1950A>C	NP_000161.2:p.Ala650=
NM_000170.3:c.1950A>C MANE Select	NP_000161.2:p.Ala650=