Canonical Allele Identifier: CA1830494138
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556669T= , CM000671.2:g.6556669T= GRCh38
NC_000009.11:g.6556669T= , CM000671.1:g.6556669T= GRCh37
NC_000009.10:g.6546669T= NCBI36
NG_016397.1:g.94024A= , LRG_643:g.94024A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2053-367A= MANE Select ENSP00000370737.4:n.2053-367A=
ENST00000638233.1:n.488-367A=
ENST00000638661.1:c.253-367A= ENSP00000491369.1:n.253-367A=
ENST00000638694.1:n.240-367A=
ENST00000639318.1:c.253-367A= ENSP00000491932.1:n.253-367A=
ENST00000639364.1:n.1753-367A=
ENST00000639443.1:n.1621-367A=
ENST00000639954.1:n.1761-367A=
ENST00000640505.1:n.292-367A=
ENST00000321612.6:c.2053-367A= ENSP00000370737.3:n.2053-367A=
NM_000170.2:c.2053-367A= , LRG_643t1:c.2053-367A= NP_000161.2:n.2053-367A=
NM_000170.3:c.2053-367A= MANE Select NP_000161.2:n.2053-367A=