Canonical Allele Identifier: CA1830496273
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558570G= , CM000671.2:g.6558570G= GRCh38
NC_000009.11:g.6558570G= , CM000671.1:g.6558570G= GRCh37
NC_000009.10:g.6548570G= NCBI36
NG_016397.1:g.92123C= , LRG_643:g.92123C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2041C= MANE Select ENSP00000370737.4:p.Leu681=
ENST00000460457.2:n.201C=
ENST00000638233.1:n.476C=
ENST00000638661.1:c.241C= ENSP00000491369.1:p.Leu81=
ENST00000638694.1:n.228C=
ENST00000639318.1:c.241C= ENSP00000491932.1:p.Leu81=
ENST00000639364.1:n.1741C=
ENST00000639443.1:n.1609C=
ENST00000639954.1:n.1749C=
ENST00000640208.1:c.241C= ENSP00000491895.1:p.Leu81=
ENST00000640505.1:n.280C=
ENST00000640592.1:n.1924C=
ENST00000321612.6:c.2041C= ENSP00000370737.3:p.Leu681=
ENST00000460457.1:n.180C=
NM_000170.2:c.2041C= , LRG_643t1:c.2041C= NP_000161.2:p.Leu681=
NM_000170.3:c.2041C= MANE Select NP_000161.2:p.Leu681=