Canonical Allele Identifier: CA1830496357
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558603C= , CM000671.2:g.6558603C= GRCh38
NC_000009.11:g.6558603C= , CM000671.1:g.6558603C= GRCh37
NC_000009.10:g.6548603C= NCBI36
NG_016397.1:g.92090G= , LRG_643:g.92090G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2008G= MANE Select ENSP00000370737.4:p.Val670=
ENST00000460457.2:n.168G=
ENST00000638233.1:n.443G=
ENST00000638661.1:c.208G= ENSP00000491369.1:p.Val70=
ENST00000638694.1:n.195G=
ENST00000639318.1:c.208G= ENSP00000491932.1:p.Val70=
ENST00000639364.1:n.1708G=
ENST00000639443.1:n.1576G=
ENST00000639954.1:n.1716G=
ENST00000640208.1:c.208G= ENSP00000491895.1:p.Val70=
ENST00000640505.1:n.247G=
ENST00000640592.1:n.1891G=
ENST00000321612.6:c.2008G= ENSP00000370737.3:p.Val670=
ENST00000460457.1:n.147G=
NM_000170.2:c.2008G= , LRG_643t1:c.2008G= NP_000161.2:p.Val670=
NM_000170.3:c.2008G= MANE Select NP_000161.2:p.Val670=