Canonical Allele Identifier: CA1830496255
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558561T= , CM000671.2:g.6558561T= GRCh38
NC_000009.11:g.6558561T= , CM000671.1:g.6558561T= GRCh37
NC_000009.10:g.6548561T= NCBI36
NG_016397.1:g.92132A= , LRG_643:g.92132A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2050A= MANE Select ENSP00000370737.4:p.Met684=
ENST00000460457.2:n.210A=
ENST00000638233.1:n.485A=
ENST00000638661.1:c.250A= ENSP00000491369.1:p.Met84=
ENST00000638694.1:n.237A=
ENST00000639318.1:c.250A= ENSP00000491932.1:p.Met84=
ENST00000639364.1:n.1750A=
ENST00000639443.1:n.1618A=
ENST00000639954.1:n.1758A=
ENST00000640208.1:c.250A= ENSP00000491895.1:p.Met84=
ENST00000640505.1:n.289A=
ENST00000640592.1:n.1933A=
ENST00000321612.6:c.2050A= ENSP00000370737.3:p.Met684=
ENST00000460457.1:n.189A=
NM_000170.2:c.2050A= , LRG_643t1:c.2050A= NP_000161.2:p.Met684=
NM_000170.3:c.2050A= MANE Select NP_000161.2:p.Met684=