Canonical Allele Identifier: CA1830503805
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6565359T= , CM000671.2:g.6565359T= GRCh38
NC_000009.11:g.6565359T= , CM000671.1:g.6565359T= GRCh37
NC_000009.10:g.6555359T= NCBI36
NG_016397.1:g.85334A= , LRG_643:g.85334A=

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.1921A= MANE Select ENSP00000370737.4:p.Arg641=
ENST00000460457.2:n.81A=
ENST00000638233.1:n.356A=
ENST00000638661.1:c.121A= ENSP00000491369.1:p.Arg41=
ENST00000638694.1:n.108A=
ENST00000639318.1:c.121A= ENSP00000491932.1:p.Arg41=
ENST00000639364.1:n.1621A=
ENST00000639443.1:n.1489A=
ENST00000639954.1:n.1629A=
ENST00000640208.1:c.121A= ENSP00000491895.1:p.Arg41=
ENST00000640505.1:n.160A=
ENST00000640592.1:n.1804A=
ENST00000321612.6:c.1921A= ENSP00000370737.3:p.Arg641=
ENST00000460457.1:n.60A=
NM_000170.2:c.1921A= , LRG_643t1:c.1921A= NP_000161.2:p.Arg641=
NM_000170.3:c.1921A= MANE Select NP_000161.2:p.Arg641=