Canonical Allele Identifier: CA1830496270
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558568G= , CM000671.2:g.6558568G= GRCh38
NC_000009.11:g.6558568G= , CM000671.1:g.6558568G= GRCh37
NC_000009.10:g.6548568G= NCBI36
NG_016397.1:g.92125C= , LRG_643:g.92125C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2043C= MANE Select ENSP00000370737.4:p.Leu681=
ENST00000460457.2:n.203C=
ENST00000638233.1:n.478C=
ENST00000638661.1:c.243C= ENSP00000491369.1:p.Leu81=
ENST00000638694.1:n.230C=
ENST00000639318.1:c.243C= ENSP00000491932.1:p.Leu81=
ENST00000639364.1:n.1743C=
ENST00000639443.1:n.1611C=
ENST00000639954.1:n.1751C=
ENST00000640208.1:c.243C= ENSP00000491895.1:p.Leu81=
ENST00000640505.1:n.282C=
ENST00000640592.1:n.1926C=
ENST00000321612.6:c.2043C= ENSP00000370737.3:p.Leu681=
ENST00000460457.1:n.182C=
NM_000170.2:c.2043C= , LRG_643t1:c.2043C= NP_000161.2:p.Leu681=
NM_000170.3:c.2043C= MANE Select NP_000161.2:p.Leu681=