Canonical Allele Identifier: CA1830496312
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558585T= , CM000671.2:g.6558585T= GRCh38
NC_000009.11:g.6558585T= , CM000671.1:g.6558585T= GRCh37
NC_000009.10:g.6548585T= NCBI36
NG_016397.1:g.92108A= , LRG_643:g.92108A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2026A= MANE Select ENSP00000370737.4:p.Ile676=
ENST00000460457.2:n.186A=
ENST00000638233.1:n.461A=
ENST00000638661.1:c.226A= ENSP00000491369.1:p.Ile76=
ENST00000638694.1:n.213A=
ENST00000639318.1:c.226A= ENSP00000491932.1:p.Ile76=
ENST00000639364.1:n.1726A=
ENST00000639443.1:n.1594A=
ENST00000639954.1:n.1734A=
ENST00000640208.1:c.226A= ENSP00000491895.1:p.Ile76=
ENST00000640505.1:n.265A=
ENST00000640592.1:n.1909A=
ENST00000321612.6:c.2026A= ENSP00000370737.3:p.Ile676=
ENST00000460457.1:n.165A=
NM_000170.2:c.2026A= , LRG_643t1:c.2026A= NP_000161.2:p.Ile676=
NM_000170.3:c.2026A= MANE Select NP_000161.2:p.Ile676=