Canonical Allele Identifier: CA372894317

Gene: GLDC

Linked Data

• COSMIC: COSM3716326
• MyVariant Identifiers: chr9:g.6595073G>T (hg19) ; chr9:g.6595073G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6595073G>T , CM000671.2:g.6595073G>T	GRCh38
NC_000009.11:g.6595073G>T , CM000671.1:g.6595073G>T	GRCh37
NC_000009.10:g.6585073G>T	NCBI36
NG_016397.1:g.55620C>A , LRG_643:g.55620C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1202C>A MANE Select	ENSP00000370737.4:p.Ser401Tyr
ENST00000638654.1:c.449C>A	ENSP00000491101.1:p.Ser150Tyr
ENST00000639364.1:n.902C>A
ENST00000639443.1:n.770C>A
ENST00000639493.1:n.354C>A
ENST00000639954.1:n.910C>A
ENST00000640592.1:n.1085C>A
ENST00000321612.6:c.1202C>A	ENSP00000370737.3:p.Ser401Tyr
ENST00000463305.1:n.286C>A
NM_000170.2:c.1202C>A , LRG_643t1:c.1202C>A	NP_000161.2:p.Ser401Tyr
NM_000170.3:c.1202C>A MANE Select	NP_000161.2:p.Ser401Tyr