Canonical Allele Identifier: CA1830496266
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558567T= , CM000671.2:g.6558567T= GRCh38
NC_000009.11:g.6558567T= , CM000671.1:g.6558567T= GRCh37
NC_000009.10:g.6548567T= NCBI36
NG_016397.1:g.92126A= , LRG_643:g.92126A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2044A= MANE Select ENSP00000370737.4:p.Lys682=
ENST00000460457.2:n.204A=
ENST00000638233.1:n.479A=
ENST00000638661.1:c.244A= ENSP00000491369.1:p.Lys82=
ENST00000638694.1:n.231A=
ENST00000639318.1:c.244A= ENSP00000491932.1:p.Lys82=
ENST00000639364.1:n.1744A=
ENST00000639443.1:n.1612A=
ENST00000639954.1:n.1752A=
ENST00000640208.1:c.244A= ENSP00000491895.1:p.Lys82=
ENST00000640505.1:n.283A=
ENST00000640592.1:n.1927A=
ENST00000321612.6:c.2044A= ENSP00000370737.3:p.Lys682=
ENST00000460457.1:n.183A=
NM_000170.2:c.2044A= , LRG_643t1:c.2044A= NP_000161.2:p.Lys682=
NM_000170.3:c.2044A= MANE Select NP_000161.2:p.Lys682=