Canonical Allele Identifier: CA263314
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 56051
ClinVar RCV Id: RCV000049460
dbSNP Id: rs386833532

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6587164_6587174del , CM000671.2:g.6587164_6587174del GRCh38
NC_000009.11:g.6587164_6587174del , CM000671.1:g.6587164_6587174del GRCh37
NC_000009.10:g.6577164_6577174del NCBI36
NG_016397.1:g.63524_63534del , LRG_643:g.63524_63534del

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1822_1832del MANE Select ENSP00000370737.4:p.Tyr608LeufsTer?
ENST00000639364.1:n.1522_1532del
ENST00000639443.1:n.1390_1400del
ENST00000639954.1:n.1530_1540del
ENST00000640592.1:n.1705_1715del
ENST00000321612.6:c.1822_1832del ENSP00000370737.3:p.Tyr608LeufsTer?
NM_000170.2:c.1822_1832del , LRG_643t1:c.1822_1832del NP_000161.2:p.Tyr608LeufsTer?
NM_000170.3:c.1822_1832del MANE Select NP_000161.2:p.Tyr608LeufsTer?