Canonical Allele Identifier: CA1830496406
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558634G= , CM000671.2:g.6558634G= GRCh38
NC_000009.11:g.6558634G= , CM000671.1:g.6558634G= GRCh37
NC_000009.10:g.6548634G= NCBI36
NG_016397.1:g.92059C= , LRG_643:g.92059C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1977C= MANE Select ENSP00000370737.4:p.His659=
ENST00000460457.2:n.137C=
ENST00000638233.1:n.412C=
ENST00000638661.1:c.177C= ENSP00000491369.1:p.His59=
ENST00000638694.1:n.164C=
ENST00000639318.1:c.177C= ENSP00000491932.1:p.His59=
ENST00000639364.1:n.1677C=
ENST00000639443.1:n.1545C=
ENST00000639954.1:n.1685C=
ENST00000640208.1:c.177C= ENSP00000491895.1:p.His59=
ENST00000640505.1:n.216C=
ENST00000640592.1:n.1860C=
ENST00000321612.6:c.1977C= ENSP00000370737.3:p.His659=
ENST00000460457.1:n.116C=
NM_000170.2:c.1977C= , LRG_643t1:c.1977C= NP_000161.2:p.His659=
NM_000170.3:c.1977C= MANE Select NP_000161.2:p.His659=