Canonical Allele Identifier: CA1830505242
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6553424T= , CM000671.2:g.6553424T= GRCh38
NC_000009.11:g.6553424T= , CM000671.1:g.6553424T= GRCh37
NC_000009.10:g.6543424T= NCBI36
NG_016397.1:g.97269A= , LRG_643:g.97269A=

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.2401A= MANE Select ENSP00000370737.4:p.Ser801=
ENST00000638233.1:n.836A=
ENST00000638661.1:c.601A= ENSP00000491369.1:p.Ser201=
ENST00000638694.1:n.588A=
ENST00000639318.1:c.601A= ENSP00000491932.1:p.Ser201=
ENST00000639364.1:n.2101A=
ENST00000639443.1:n.1969A=
ENST00000639639.1:c.103A= ENSP00000491312.1:p.Ser35=
ENST00000639954.1:n.2109A=
ENST00000640505.1:n.640A=
ENST00000321612.6:c.2401A= ENSP00000370737.3:p.Ser801=
NM_000170.2:c.2401A= , LRG_643t1:c.2401A= NP_000161.2:p.Ser801=
NM_000170.3:c.2401A= MANE Select NP_000161.2:p.Ser801=