Canonical Allele Identifier: CA372876184
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6550862G>A , CM000671.2:g.6550862G>A GRCh38
NC_000009.11:g.6550862G>A , CM000671.1:g.6550862G>A GRCh37
NC_000009.10:g.6540862G>A NCBI36
NG_016397.1:g.99831C>T , LRG_643:g.99831C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2510C>T MANE Select ENSP00000370737.4:p.Ala837Val
ENST00000638233.1:n.945C>T
ENST00000638661.1:c.710C>T ENSP00000491369.1:p.Ala237Val
ENST00000638694.1:n.697C>T
ENST00000639318.1:c.710C>T ENSP00000491932.1:p.Ala237Val
ENST00000639364.1:n.2210C>T
ENST00000639443.1:n.2078C>T
ENST00000639639.1:c.212C>T ENSP00000491312.1:p.Ala71Val
ENST00000639954.1:n.2218C>T
ENST00000640505.1:n.749C>T
ENST00000321612.6:c.2510C>T ENSP00000370737.3:p.Ala837Val
NM_000170.2:c.2510C>T , LRG_643t1:c.2510C>T NP_000161.2:p.Ala837Val
NM_000170.3:c.2510C>T MANE Select NP_000161.2:p.Ala837Val