Canonical Allele Identifier: CA1830496476
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558671G= , CM000671.2:g.6558671G= GRCh38
NC_000009.11:g.6558671G= , CM000671.1:g.6558671G= GRCh37
NC_000009.10:g.6548671G= NCBI36
NG_016397.1:g.92022C= , LRG_643:g.92022C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1940C= MANE Select ENSP00000370737.4:p.Pro647=
ENST00000460457.2:n.100C=
ENST00000638233.1:n.375C=
ENST00000638661.1:c.140C= ENSP00000491369.1:p.Pro47=
ENST00000638694.1:n.127C=
ENST00000639318.1:c.140C= ENSP00000491932.1:p.Pro47=
ENST00000639364.1:n.1640C=
ENST00000639443.1:n.1508C=
ENST00000639954.1:n.1648C=
ENST00000640208.1:c.140C= ENSP00000491895.1:p.Pro47=
ENST00000640505.1:n.179C=
ENST00000640592.1:n.1823C=
ENST00000321612.6:c.1940C= ENSP00000370737.3:p.Pro647=
ENST00000460457.1:n.79C=
NM_000170.2:c.1940C= , LRG_643t1:c.1940C= NP_000161.2:p.Pro647=
NM_000170.3:c.1940C= MANE Select NP_000161.2:p.Pro647=