Canonical Allele Identifier: CA1830496500
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558680C= , CM000671.2:g.6558680C= GRCh38
NC_000009.11:g.6558680C= , CM000671.1:g.6558680C= GRCh37
NC_000009.10:g.6548680C= NCBI36
NG_016397.1:g.92013G= , LRG_643:g.92013G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1931G= MANE Select ENSP00000370737.4:p.Cys644=
ENST00000460457.2:n.91G=
ENST00000638233.1:n.366G=
ENST00000638661.1:c.131G= ENSP00000491369.1:p.Cys44=
ENST00000638694.1:n.118G=
ENST00000639318.1:c.131G= ENSP00000491932.1:p.Cys44=
ENST00000639364.1:n.1631G=
ENST00000639443.1:n.1499G=
ENST00000639954.1:n.1639G=
ENST00000640208.1:c.131G= ENSP00000491895.1:p.Cys44=
ENST00000640505.1:n.170G=
ENST00000640592.1:n.1814G=
ENST00000321612.6:c.1931G= ENSP00000370737.3:p.Cys644=
ENST00000460457.1:n.70G=
NM_000170.2:c.1931G= , LRG_643t1:c.1931G= NP_000161.2:p.Cys644=
NM_000170.3:c.1931G= MANE Select NP_000161.2:p.Cys644=