Canonical Allele Identifier: CA1830496459
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558659T= , CM000671.2:g.6558659T= GRCh38
NC_000009.11:g.6558659T= , CM000671.1:g.6558659T= GRCh37
NC_000009.10:g.6548659T= NCBI36
NG_016397.1:g.92034A= , LRG_643:g.92034A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1952A= MANE Select ENSP00000370737.4:p.His651=
ENST00000460457.2:n.112A=
ENST00000638233.1:n.387A=
ENST00000638661.1:c.152A= ENSP00000491369.1:p.His51=
ENST00000638694.1:n.139A=
ENST00000639318.1:c.152A= ENSP00000491932.1:p.His51=
ENST00000639364.1:n.1652A=
ENST00000639443.1:n.1520A=
ENST00000639954.1:n.1660A=
ENST00000640208.1:c.152A= ENSP00000491895.1:p.His51=
ENST00000640505.1:n.191A=
ENST00000640592.1:n.1835A=
ENST00000321612.6:c.1952A= ENSP00000370737.3:p.His651=
ENST00000460457.1:n.91A=
NM_000170.2:c.1952A= , LRG_643t1:c.1952A= NP_000161.2:p.His651=
NM_000170.3:c.1952A= MANE Select NP_000161.2:p.His651=