Canonical Allele Identifier: CA1830496185
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558528C= , CM000671.2:g.6558528C= GRCh38
NC_000009.11:g.6558528C= , CM000671.1:g.6558528C= GRCh37
NC_000009.10:g.6548528C= NCBI36
NG_016397.1:g.92165G= , LRG_643:g.92165G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2052+31G= MANE Select ENSP00000370737.4:n.2052+31G=
ENST00000460457.2:n.212+31G=
ENST00000638233.1:n.487+31G=
ENST00000638661.1:c.252+31G= ENSP00000491369.1:n.252+31G=
ENST00000638694.1:n.239+31G=
ENST00000639318.1:c.252+31G= ENSP00000491932.1:n.252+31G=
ENST00000639364.1:n.1752+31G=
ENST00000639443.1:n.1620+31G=
ENST00000639954.1:n.1760+31G=
ENST00000640208.1:c.283G= ENSP00000491895.1:p.Gly95=
ENST00000640505.1:n.291+31G=
ENST00000640592.1:n.1966G=
ENST00000321612.6:c.2052+31G= ENSP00000370737.3:n.2052+31G=
ENST00000460457.1:n.222G=
NM_000170.2:c.2052+31G= , LRG_643t1:c.2052+31G= NP_000161.2:n.2052+31G=
NM_000170.3:c.2052+31G= MANE Select NP_000161.2:n.2052+31G=