Canonical Allele Identifier: CA372881367

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556251T>G (hg19) ; chr9:g.6556251T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556251T>G , CM000671.2:g.6556251T>G	GRCh38
NC_000009.11:g.6556251T>G , CM000671.1:g.6556251T>G	GRCh37
NC_000009.10:g.6546251T>G	NCBI36
NG_016397.1:g.94442A>C , LRG_643:g.94442A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2104A>C MANE Select	ENSP00000370737.4:p.Thr702Pro
ENST00000638233.1:n.539A>C
ENST00000638661.1:c.304A>C	ENSP00000491369.1:p.Thr102Pro
ENST00000638694.1:n.291A>C
ENST00000639318.1:c.304A>C	ENSP00000491932.1:p.Thr102Pro
ENST00000639364.1:n.1804A>C
ENST00000639443.1:n.1672A>C
ENST00000639954.1:n.1812A>C
ENST00000640505.1:n.343A>C
ENST00000321612.6:c.2104A>C	ENSP00000370737.3:p.Thr702Pro
NM_000170.2:c.2104A>C , LRG_643t1:c.2104A>C	NP_000161.2:p.Thr702Pro
NM_000170.3:c.2104A>C MANE Select	NP_000161.2:p.Thr702Pro