Canonical Allele Identifier: CA1830496745
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558926C= , CM000671.2:g.6558926C= GRCh38
NC_000009.11:g.6558926C= , CM000671.1:g.6558926C= GRCh37
NC_000009.10:g.6548926C= NCBI36
NG_016397.1:g.91767G= , LRG_643:g.91767G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1927-242G= MANE Select ENSP00000370737.4:n.1927-242G=
ENST00000460457.2:n.87-242G=
ENST00000638233.1:n.362-242G=
ENST00000638661.1:c.127-242G= ENSP00000491369.1:n.127-242G=
ENST00000638694.1:n.114-242G=
ENST00000639318.1:c.127-242G= ENSP00000491932.1:n.127-242G=
ENST00000639364.1:n.1627-242G=
ENST00000639443.1:n.1495-242G=
ENST00000639954.1:n.1635-242G=
ENST00000640208.1:c.127-242G= ENSP00000491895.1:n.127-242G=
ENST00000640505.1:n.166-242G=
ENST00000640592.1:n.1810-242G=
ENST00000321612.6:c.1927-242G= ENSP00000370737.3:n.1927-242G=
ENST00000460457.1:n.66-242G=
NM_000170.2:c.1927-242G= , LRG_643t1:c.1927-242G= NP_000161.2:n.1927-242G=
NM_000170.3:c.1927-242G= MANE Select NP_000161.2:n.1927-242G=