Canonical Allele Identifier: CA1830507374
Community Standard Title: NM_000170.3(GLDC):c.2281G= (p.Gly761=)
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6554703C= , CM000671.2:g.6554703C= GRCh38
NC_000009.11:g.6554703C= , CM000671.1:g.6554703C= GRCh37
NC_000009.10:g.6544703C= NCBI36
NG_016397.1:g.95990G= , LRG_643:g.95990G=

Transcript Alleles

HGVS Amino-acid Change
NM_000170.3:c.2281G= MANE Select NP_000161.2:p.Gly761=
ENST00000321612.8:c.2281G= MANE Select ENSP00000370737.4:p.Gly761=
NM_000170.2:c.2281G= , LRG_643t1:c.2281G= NP_000161.2:p.Gly761=
ENST00000321612.6:c.2281G= ENSP00000370737.3:p.Gly761=
ENST00000467946.1:n.207G=
ENST00000638233.1:n.716G=
ENST00000638661.1:c.481G= ENSP00000491369.1:p.Gly161=
ENST00000638694.1:n.468G=
ENST00000639318.1:c.481G= ENSP00000491932.1:p.Gly161=
ENST00000639364.1:n.1981G=
ENST00000639443.1:n.1849G=
ENST00000639639.1:c.-18G= ENSP00000491312.1:n.-18G=
ENST00000639954.1:n.1989G=
ENST00000640505.1:n.520G=