Canonical Allele Identifier: CA913183013

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556228dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556228dup , CM000671.2:g.6556228dup	GRCh38
NC_000009.11:g.6556228dup , CM000671.1:g.6556228dup	GRCh37
NC_000009.10:g.6546228dup	NCBI36
NG_016397.1:g.94465dup , LRG_643:g.94465dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2127dup MANE Select	ENSP00000370737.4:p.Ile710HisfsTer3
ENST00000638233.1:n.562dup
ENST00000638661.1:c.327dup	ENSP00000491369.1:p.Ile110HisfsTer3
ENST00000638694.1:n.314dup
ENST00000639318.1:c.327dup	ENSP00000491932.1:p.Ile110HisfsTer3
ENST00000639364.1:n.1827dup
ENST00000639443.1:n.1695dup
ENST00000639954.1:n.1835dup
ENST00000640505.1:n.366dup
ENST00000321612.6:c.2127dup	ENSP00000370737.3:p.Ile710HisfsTer3
NM_000170.2:c.2127dup , LRG_643t1:c.2127dup	NP_000161.2:p.Ile710HisfsTer3
NM_000170.3:c.2127dup MANE Select	NP_000161.2:p.Ile710HisfsTer3