Canonical Allele Identifier: CA1830496347
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558598A= , CM000671.2:g.6558598A= GRCh38
NC_000009.11:g.6558598A= , CM000671.1:g.6558598A= GRCh37
NC_000009.10:g.6548598A= NCBI36
NG_016397.1:g.92095T= , LRG_643:g.92095T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2013T= MANE Select ENSP00000370737.4:p.Asp671=
ENST00000460457.2:n.173T=
ENST00000638233.1:n.448T=
ENST00000638661.1:c.213T= ENSP00000491369.1:p.Asp71=
ENST00000638694.1:n.200T=
ENST00000639318.1:c.213T= ENSP00000491932.1:p.Asp71=
ENST00000639364.1:n.1713T=
ENST00000639443.1:n.1581T=
ENST00000639954.1:n.1721T=
ENST00000640208.1:c.213T= ENSP00000491895.1:p.Asp71=
ENST00000640505.1:n.252T=
ENST00000640592.1:n.1896T=
ENST00000321612.6:c.2013T= ENSP00000370737.3:p.Asp671=
ENST00000460457.1:n.152T=
NM_000170.2:c.2013T= , LRG_643t1:c.2013T= NP_000161.2:p.Asp671=
NM_000170.3:c.2013T= MANE Select NP_000161.2:p.Asp671=