Canonical Allele Identifier: CA918403270
Gene: GLDC HGNC NCBI

Linked Data

dbSNP Id: rs1563835665

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6555945del , CM000671.2:g.6555945del GRCh38
NC_000009.11:g.6555945del , CM000671.1:g.6555945del GRCh37
NC_000009.10:g.6545945del NCBI36
NG_016397.1:g.94750del , LRG_643:g.94750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2202+210del MANE Select ENSP00000370737.4:n.2202+210del
ENST00000638233.1:n.637+210del
ENST00000638661.1:c.402+210del ENSP00000491369.1:n.402+210del
ENST00000638694.1:n.389+210del
ENST00000639318.1:c.402+210del ENSP00000491932.1:n.402+210del
ENST00000639364.1:n.1902+210del
ENST00000639443.1:n.1770+210del
ENST00000639954.1:n.1910+210del
ENST00000640505.1:n.441+210del
ENST00000321612.6:c.2202+210del ENSP00000370737.3:n.2202+210del
NM_000170.2:c.2202+210del , LRG_643t1:c.2202+210del NP_000161.2:n.2202+210del
NM_000170.3:c.2202+210del MANE Select NP_000161.2:n.2202+210del