Canonical Allele Identifier: CA1830496538
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558728A= , CM000671.2:g.6558728A= GRCh38
NC_000009.11:g.6558728A= , CM000671.1:g.6558728A= GRCh37
NC_000009.10:g.6548728A= NCBI36
NG_016397.1:g.91965T= , LRG_643:g.91965T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1927-44T= MANE Select ENSP00000370737.4:n.1927-44T=
ENST00000460457.2:n.87-44T=
ENST00000638233.1:n.362-44T=
ENST00000638661.1:c.127-44T= ENSP00000491369.1:n.127-44T=
ENST00000638694.1:n.114-44T=
ENST00000639318.1:c.127-44T= ENSP00000491932.1:n.127-44T=
ENST00000639364.1:n.1627-44T=
ENST00000639443.1:n.1495-44T=
ENST00000639954.1:n.1635-44T=
ENST00000640208.1:c.127-44T= ENSP00000491895.1:n.127-44T=
ENST00000640505.1:n.166-44T=
ENST00000640592.1:n.1810-44T=
ENST00000321612.6:c.1927-44T= ENSP00000370737.3:n.1927-44T=
ENST00000460457.1:n.66-44T=
NM_000170.2:c.1927-44T= , LRG_643t1:c.1927-44T= NP_000161.2:n.1927-44T=
NM_000170.3:c.1927-44T= MANE Select NP_000161.2:n.1927-44T=