Canonical Allele Identifier: CA1830493149
Gene: GLDC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556018C= , CM000671.2:g.6556018C= GRCh38
NC_000009.11:g.6556018C= , CM000671.1:g.6556018C= GRCh37
NC_000009.10:g.6546018C= NCBI36
NG_016397.1:g.94675G= , LRG_643:g.94675G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2202+135G= MANE Select ENSP00000370737.4:n.2202+135G=
ENST00000638233.1:n.637+135G=
ENST00000638661.1:c.402+135G= ENSP00000491369.1:n.402+135G=
ENST00000638694.1:n.389+135G=
ENST00000639318.1:c.402+135G= ENSP00000491932.1:n.402+135G=
ENST00000639364.1:n.1902+135G=
ENST00000639443.1:n.1770+135G=
ENST00000639954.1:n.1910+135G=
ENST00000640505.1:n.441+135G=
ENST00000321612.6:c.2202+135G= ENSP00000370737.3:n.2202+135G=
NM_000170.2:c.2202+135G= , LRG_643t1:c.2202+135G= NP_000161.2:n.2202+135G=
NM_000170.3:c.2202+135G= MANE Select NP_000161.2:n.2202+135G=
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