Canonical Allele Identifier: CA463585508

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556171C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556171C>A , CM000671.2:g.6556171C>A	GRCh38
NC_000009.11:g.6556171C>A , CM000671.1:g.6556171C>A	GRCh37
NC_000009.10:g.6546171C>A	NCBI36
NG_016397.1:g.94522G>T , LRG_643:g.94522G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2184G>T MANE Select	ENSP00000370737.4:p.Gly728=
ENST00000638233.1:n.619G>T
ENST00000638661.1:c.384G>T	ENSP00000491369.1:p.Gly128=
ENST00000638694.1:n.371G>T
ENST00000639318.1:c.384G>T	ENSP00000491932.1:p.Gly128=
ENST00000639364.1:n.1884G>T
ENST00000639443.1:n.1752G>T
ENST00000639954.1:n.1892G>T
ENST00000640505.1:n.423G>T
ENST00000321612.6:c.2184G>T	ENSP00000370737.3:p.Gly728=
NM_000170.2:c.2184G>T , LRG_643t1:c.2184G>T	NP_000161.2:p.Gly728=
NM_000170.3:c.2184G>T MANE Select	NP_000161.2:p.Gly728=