Canonical Allele Identifier: CA1830496471
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558670C= , CM000671.2:g.6558670C= GRCh38
NC_000009.11:g.6558670C= , CM000671.1:g.6558670C= GRCh37
NC_000009.10:g.6548670C= NCBI36
NG_016397.1:g.92023G= , LRG_643:g.92023G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1941G= MANE Select ENSP00000370737.4:p.Pro647=
ENST00000460457.2:n.101G=
ENST00000638233.1:n.376G=
ENST00000638661.1:c.141G= ENSP00000491369.1:p.Pro47=
ENST00000638694.1:n.128G=
ENST00000639318.1:c.141G= ENSP00000491932.1:p.Pro47=
ENST00000639364.1:n.1641G=
ENST00000639443.1:n.1509G=
ENST00000639954.1:n.1649G=
ENST00000640208.1:c.141G= ENSP00000491895.1:p.Pro47=
ENST00000640505.1:n.180G=
ENST00000640592.1:n.1824G=
ENST00000321612.6:c.1941G= ENSP00000370737.3:p.Pro647=
ENST00000460457.1:n.80G=
NM_000170.2:c.1941G= , LRG_643t1:c.1941G= NP_000161.2:p.Pro647=
NM_000170.3:c.1941G= MANE Select NP_000161.2:p.Pro647=