Canonical Allele Identifier: CA1830493485
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556210G= , CM000671.2:g.6556210G= GRCh38
NC_000009.11:g.6556210G= , CM000671.1:g.6556210G= GRCh37
NC_000009.10:g.6546210G= NCBI36
NG_016397.1:g.94483C= , LRG_643:g.94483C=

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.2145C= MANE Select ENSP00000370737.4:p.Asp715=
ENST00000638233.1:n.580C=
ENST00000638661.1:c.345C= ENSP00000491369.1:p.Asp115=
ENST00000638694.1:n.332C=
ENST00000639318.1:c.345C= ENSP00000491932.1:p.Asp115=
ENST00000639364.1:n.1845C=
ENST00000639443.1:n.1713C=
ENST00000639954.1:n.1853C=
ENST00000640505.1:n.384C=
ENST00000321612.6:c.2145C= ENSP00000370737.3:p.Asp715=
NM_000170.2:c.2145C= , LRG_643t1:c.2145C= NP_000161.2:p.Asp715=
NM_000170.3:c.2145C= MANE Select NP_000161.2:p.Asp715=