Canonical Allele Identifier: CA1830496306
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558583G= , CM000671.2:g.6558583G= GRCh38
NC_000009.11:g.6558583G= , CM000671.1:g.6558583G= GRCh37
NC_000009.10:g.6548583G= NCBI36
NG_016397.1:g.92110C= , LRG_643:g.92110C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2028C= MANE Select ENSP00000370737.4:p.Ile676=
ENST00000460457.2:n.188C=
ENST00000638233.1:n.463C=
ENST00000638661.1:c.228C= ENSP00000491369.1:p.Ile76=
ENST00000638694.1:n.215C=
ENST00000639318.1:c.228C= ENSP00000491932.1:p.Ile76=
ENST00000639364.1:n.1728C=
ENST00000639443.1:n.1596C=
ENST00000639954.1:n.1736C=
ENST00000640208.1:c.228C= ENSP00000491895.1:p.Ile76=
ENST00000640505.1:n.267C=
ENST00000640592.1:n.1911C=
ENST00000321612.6:c.2028C= ENSP00000370737.3:p.Ile676=
ENST00000460457.1:n.167C=
NM_000170.2:c.2028C= , LRG_643t1:c.2028C= NP_000161.2:p.Ile676=
NM_000170.3:c.2028C= MANE Select NP_000161.2:p.Ile676=