Canonical Allele Identifier: CA1830496338
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558593T= , CM000671.2:g.6558593T= GRCh38
NC_000009.11:g.6558593T= , CM000671.1:g.6558593T= GRCh37
NC_000009.10:g.6548593T= NCBI36
NG_016397.1:g.92100A= , LRG_643:g.92100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2018A= MANE Select ENSP00000370737.4:p.Tyr673=
ENST00000460457.2:n.178A=
ENST00000638233.1:n.453A=
ENST00000638661.1:c.218A= ENSP00000491369.1:p.Tyr73=
ENST00000638694.1:n.205A=
ENST00000639318.1:c.218A= ENSP00000491932.1:p.Tyr73=
ENST00000639364.1:n.1718A=
ENST00000639443.1:n.1586A=
ENST00000639954.1:n.1726A=
ENST00000640208.1:c.218A= ENSP00000491895.1:p.Tyr73=
ENST00000640505.1:n.257A=
ENST00000640592.1:n.1901A=
ENST00000321612.6:c.2018A= ENSP00000370737.3:p.Tyr673=
ENST00000460457.1:n.157A=
NM_000170.2:c.2018A= , LRG_643t1:c.2018A= NP_000161.2:p.Tyr673=
NM_000170.3:c.2018A= MANE Select NP_000161.2:p.Tyr673=