Canonical Allele Identifier: CA1830496294
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558579C= , CM000671.2:g.6558579C= GRCh38
NC_000009.11:g.6558579C= , CM000671.1:g.6558579C= GRCh37
NC_000009.10:g.6548579C= NCBI36
NG_016397.1:g.92114G= , LRG_643:g.92114G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2032G= MANE Select ENSP00000370737.4:p.Ala678=
ENST00000460457.2:n.192G=
ENST00000638233.1:n.467G=
ENST00000638661.1:c.232G= ENSP00000491369.1:p.Ala78=
ENST00000638694.1:n.219G=
ENST00000639318.1:c.232G= ENSP00000491932.1:p.Ala78=
ENST00000639364.1:n.1732G=
ENST00000639443.1:n.1600G=
ENST00000639954.1:n.1740G=
ENST00000640208.1:c.232G= ENSP00000491895.1:p.Ala78=
ENST00000640505.1:n.271G=
ENST00000640592.1:n.1915G=
ENST00000321612.6:c.2032G= ENSP00000370737.3:p.Ala678=
ENST00000460457.1:n.171G=
NM_000170.2:c.2032G= , LRG_643t1:c.2032G= NP_000161.2:p.Ala678=
NM_000170.3:c.2032G= MANE Select NP_000161.2:p.Ala678=