Canonical Allele Identifier: CA1830491599
Community Standard Title: NM_000170.3(GLDC):c.2216G= (p.Arg739=)
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6554768C= , CM000671.2:g.6554768C= GRCh38
NC_000009.11:g.6554768C= , CM000671.1:g.6554768C= GRCh37
NC_000009.10:g.6544768C= NCBI36
NG_016397.1:g.95925G= , LRG_643:g.95925G=

Transcript Alleles

HGVS Amino-acid Change
NM_000170.3:c.2216G= MANE Select NP_000161.2:p.Arg739=
ENST00000321612.8:c.2216G= MANE Select ENSP00000370737.4:p.Arg739=
NM_000170.2:c.2216G= , LRG_643t1:c.2216G= NP_000161.2:p.Arg739=
ENST00000321612.6:c.2216G= ENSP00000370737.3:p.Arg739=
ENST00000467946.1:n.142G=
ENST00000638233.1:n.651G=
ENST00000638661.1:c.416G= ENSP00000491369.1:p.Arg139=
ENST00000638694.1:n.403G=
ENST00000639318.1:c.416G= ENSP00000491932.1:p.Arg139=
ENST00000639364.1:n.1916G=
ENST00000639443.1:n.1784G=
ENST00000639639.1:c.-83G= ENSP00000491312.1:n.-83G=
ENST00000639954.1:n.1924G=
ENST00000640505.1:n.455G=