Canonical Allele Identifier: CA1830494111
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556645T= , CM000671.2:g.6556645T= GRCh38
NC_000009.11:g.6556645T= , CM000671.1:g.6556645T= GRCh37
NC_000009.10:g.6546645T= NCBI36
NG_016397.1:g.94048A= , LRG_643:g.94048A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2053-343A= MANE Select ENSP00000370737.4:n.2053-343A=
ENST00000638233.1:n.488-343A=
ENST00000638661.1:c.253-343A= ENSP00000491369.1:n.253-343A=
ENST00000638694.1:n.240-343A=
ENST00000639318.1:c.253-343A= ENSP00000491932.1:n.253-343A=
ENST00000639364.1:n.1753-343A=
ENST00000639443.1:n.1621-343A=
ENST00000639954.1:n.1761-343A=
ENST00000640505.1:n.292-343A=
ENST00000321612.6:c.2053-343A= ENSP00000370737.3:n.2053-343A=
NM_000170.2:c.2053-343A= , LRG_643t1:c.2053-343A= NP_000161.2:n.2053-343A=
NM_000170.3:c.2053-343A= MANE Select NP_000161.2:n.2053-343A=