Canonical Allele Identifier: CA913183014

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6556266_6556274del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556266_6556274del , CM000671.2:g.6556266_6556274del	GRCh38
NC_000009.11:g.6556266_6556274del , CM000671.1:g.6556266_6556274del	GRCh37
NC_000009.10:g.6546266_6546274del	NCBI36
NG_016397.1:g.94419_94427del , LRG_643:g.94419_94427del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2081_2089del MANE Select	ENSP00000370737.4:p.Ala694_Ile697delinsVal
ENST00000638233.1:n.516_524del
ENST00000638661.1:c.281_289del	ENSP00000491369.1:p.Ala94_Ile97delinsVal
ENST00000638694.1:n.268_276del
ENST00000639318.1:c.281_289del	ENSP00000491932.1:p.Ala94_Ile97delinsVal
ENST00000639364.1:n.1781_1789del
ENST00000639443.1:n.1649_1657del
ENST00000639954.1:n.1789_1797del
ENST00000640505.1:n.320_328del
ENST00000321612.6:c.2081_2089del	ENSP00000370737.3:p.Ala694_Ile697delinsVal
NM_000170.2:c.2081_2089del , LRG_643t1:c.2081_2089del	NP_000161.2:p.Ala694_Ile697delinsVal
NM_000170.3:c.2081_2089del MANE Select	NP_000161.2:p.Ala694_Ile697delinsVal