Canonical Allele Identifier: CA1830493074
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6555959C= , CM000671.2:g.6555959C= GRCh38
NC_000009.11:g.6555959C= , CM000671.1:g.6555959C= GRCh37
NC_000009.10:g.6545959C= NCBI36
NG_016397.1:g.94734G= , LRG_643:g.94734G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2202+194G= MANE Select ENSP00000370737.4:n.2202+194G=
ENST00000638233.1:n.637+194G=
ENST00000638661.1:c.402+194G= ENSP00000491369.1:n.402+194G=
ENST00000638694.1:n.389+194G=
ENST00000639318.1:c.402+194G= ENSP00000491932.1:n.402+194G=
ENST00000639364.1:n.1902+194G=
ENST00000639443.1:n.1770+194G=
ENST00000639954.1:n.1910+194G=
ENST00000640505.1:n.441+194G=
ENST00000321612.6:c.2202+194G= ENSP00000370737.3:n.2202+194G=
NM_000170.2:c.2202+194G= , LRG_643t1:c.2202+194G= NP_000161.2:n.2202+194G=
NM_000170.3:c.2202+194G= MANE Select NP_000161.2:n.2202+194G=