Canonical Allele Identifier: CA1830493349
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556159A= , CM000671.2:g.6556159A= GRCh38
NC_000009.11:g.6556159A= , CM000671.1:g.6556159A= GRCh37
NC_000009.10:g.6546159A= NCBI36
NG_016397.1:g.94534T= , LRG_643:g.94534T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2196T= MANE Select ENSP00000370737.4:p.Asn732=
ENST00000638233.1:n.631T=
ENST00000638661.1:c.396T= ENSP00000491369.1:p.Asn132=
ENST00000638694.1:n.383T=
ENST00000639318.1:c.396T= ENSP00000491932.1:p.Asn132=
ENST00000639364.1:n.1896T=
ENST00000639443.1:n.1764T=
ENST00000639954.1:n.1904T=
ENST00000640505.1:n.435T=
ENST00000321612.6:c.2196T= ENSP00000370737.3:p.Asn732=
NM_000170.2:c.2196T= , LRG_643t1:c.2196T= NP_000161.2:p.Asn732=
NM_000170.3:c.2196T= MANE Select NP_000161.2:p.Asn732=