Canonical Allele Identifier: CA1830496415
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558637G= , CM000671.2:g.6558637G= GRCh38
NC_000009.11:g.6558637G= , CM000671.1:g.6558637G= GRCh37
NC_000009.10:g.6548637G= NCBI36
NG_016397.1:g.92056C= , LRG_643:g.92056C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1974C= MANE Select ENSP00000370737.4:p.Ala658=
ENST00000460457.2:n.134C=
ENST00000638233.1:n.409C=
ENST00000638661.1:c.174C= ENSP00000491369.1:p.Ala58=
ENST00000638694.1:n.161C=
ENST00000639318.1:c.174C= ENSP00000491932.1:p.Ala58=
ENST00000639364.1:n.1674C=
ENST00000639443.1:n.1542C=
ENST00000639954.1:n.1682C=
ENST00000640208.1:c.174C= ENSP00000491895.1:p.Ala58=
ENST00000640505.1:n.213C=
ENST00000640592.1:n.1857C=
ENST00000321612.6:c.1974C= ENSP00000370737.3:p.Ala658=
ENST00000460457.1:n.113C=
NM_000170.2:c.1974C= , LRG_643t1:c.1974C= NP_000161.2:p.Ala658=
NM_000170.3:c.1974C= MANE Select NP_000161.2:p.Ala658=