Canonical Allele Identifier: CA1830496586
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558780G= , CM000671.2:g.6558780G= GRCh38
NC_000009.11:g.6558780G= , CM000671.1:g.6558780G= GRCh37
NC_000009.10:g.6548780G= NCBI36
NG_016397.1:g.91913C= , LRG_643:g.91913C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1927-96C= MANE Select ENSP00000370737.4:n.1927-96C=
ENST00000460457.2:n.87-96C=
ENST00000638233.1:n.362-96C=
ENST00000638661.1:c.127-96C= ENSP00000491369.1:n.127-96C=
ENST00000638694.1:n.114-96C=
ENST00000639318.1:c.127-96C= ENSP00000491932.1:n.127-96C=
ENST00000639364.1:n.1627-96C=
ENST00000639443.1:n.1495-96C=
ENST00000639954.1:n.1635-96C=
ENST00000640208.1:c.127-96C= ENSP00000491895.1:n.127-96C=
ENST00000640505.1:n.166-96C=
ENST00000640592.1:n.1810-96C=
ENST00000321612.6:c.1927-96C= ENSP00000370737.3:n.1927-96C=
ENST00000460457.1:n.66-96C=
NM_000170.2:c.1927-96C= , LRG_643t1:c.1927-96C= NP_000161.2:n.1927-96C=
NM_000170.3:c.1927-96C= MANE Select NP_000161.2:n.1927-96C=