Canonical Allele Identifier: CA1830493582
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556255T= , CM000671.2:g.6556255T= GRCh38
NC_000009.11:g.6556255T= , CM000671.1:g.6556255T= GRCh37
NC_000009.10:g.6546255T= NCBI36
NG_016397.1:g.94438A= , LRG_643:g.94438A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2100A= MANE Select ENSP00000370737.4:p.Pro700=
ENST00000638233.1:n.535A=
ENST00000638661.1:c.300A= ENSP00000491369.1:p.Pro100=
ENST00000638694.1:n.287A=
ENST00000639318.1:c.300A= ENSP00000491932.1:p.Pro100=
ENST00000639364.1:n.1800A=
ENST00000639443.1:n.1668A=
ENST00000639954.1:n.1808A=
ENST00000640505.1:n.339A=
ENST00000321612.6:c.2100A= ENSP00000370737.3:p.Pro700=
NM_000170.2:c.2100A= , LRG_643t1:c.2100A= NP_000161.2:p.Pro700=
NM_000170.3:c.2100A= MANE Select NP_000161.2:p.Pro700=