Canonical Allele Identifier: CA1830494002
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556555G= , CM000671.2:g.6556555G= GRCh38
NC_000009.11:g.6556555G= , CM000671.1:g.6556555G= GRCh37
NC_000009.10:g.6546555G= NCBI36
NG_016397.1:g.94138C= , LRG_643:g.94138C=

Transcript Alleles

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