Canonical Allele Identifier: CA372882169
Gene: GLDC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558669T>C , CM000671.2:g.6558669T>C GRCh38
NC_000009.11:g.6558669T>C , CM000671.1:g.6558669T>C GRCh37
NC_000009.10:g.6548669T>C NCBI36
NG_016397.1:g.92024A>G , LRG_643:g.92024A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1942A>G MANE Select ENSP00000370737.4:p.Lys648Glu
ENST00000460457.2:n.102A>G
ENST00000638233.1:n.377A>G
ENST00000638661.1:c.142A>G ENSP00000491369.1:p.Lys48Glu
ENST00000638694.1:n.129A>G
ENST00000639318.1:c.142A>G ENSP00000491932.1:p.Lys48Glu
ENST00000639364.1:n.1642A>G
ENST00000639443.1:n.1510A>G
ENST00000639954.1:n.1650A>G
ENST00000640208.1:c.142A>G ENSP00000491895.1:p.Lys48Glu
ENST00000640505.1:n.181A>G
ENST00000640592.1:n.1825A>G
ENST00000321612.6:c.1942A>G ENSP00000370737.3:p.Lys648Glu
ENST00000460457.1:n.81A>G
NM_000170.2:c.1942A>G , LRG_643t1:c.1942A>G NP_000161.2:p.Lys648Glu
NM_000170.3:c.1942A>G MANE Select NP_000161.2:p.Lys648Glu