Canonical Allele Identifier: CA1830493844
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556420_6556421delinsTG , CM000671.2:g.6556420_6556421delinsTG GRCh38
NC_000009.11:g.6556420_6556421delinsTG , CM000671.1:g.6556420_6556421delinsTG GRCh37
NC_000009.10:g.6546420_6546421delinsTG NCBI36
NG_016397.1:g.94272_94273delinsCA , LRG_643:g.94272_94273delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2053-119_2053-118delinsCA MANE Select ENSP00000370737.4:n.2053-119_2053-118delinsCA
ENST00000638233.1:n.488-119_488-118delinsCA
ENST00000638661.1:c.253-119_253-118delinsCA ENSP00000491369.1:n.253-119_253-118delinsCA
ENST00000638694.1:n.240-119_240-118delinsCA
ENST00000639318.1:c.253-119_253-118delinsCA ENSP00000491932.1:n.253-119_253-118delinsCA
ENST00000639364.1:n.1753-119_1753-118delinsCA
ENST00000639443.1:n.1621-119_1621-118delinsCA
ENST00000639954.1:n.1761-119_1761-118delinsCA
ENST00000640505.1:n.292-119_292-118delinsCA
ENST00000321612.6:c.2053-119_2053-118delinsCA ENSP00000370737.3:n.2053-119_2053-118delinsCA
NM_000170.2:c.2053-119_2053-118delinsCA , LRG_643t1:c.2053-119_2053-118delinsCA NP_000161.2:n.2053-119_2053-118delinsCA
NM_000170.3:c.2053-119_2053-118delinsCA MANE Select NP_000161.2:n.2053-119_2053-118delinsCA