Canonical Allele Identifier: CA1830493681
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556295T= , CM000671.2:g.6556295T= GRCh38
NC_000009.11:g.6556295T= , CM000671.1:g.6556295T= GRCh37
NC_000009.10:g.6546295T= NCBI36
NG_016397.1:g.94398A= , LRG_643:g.94398A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2060A= MANE Select ENSP00000370737.4:p.Lys687=
ENST00000638233.1:n.495A=
ENST00000638661.1:c.260A= ENSP00000491369.1:p.Lys87=
ENST00000638694.1:n.247A=
ENST00000639318.1:c.260A= ENSP00000491932.1:p.Lys87=
ENST00000639364.1:n.1760A=
ENST00000639443.1:n.1628A=
ENST00000639954.1:n.1768A=
ENST00000640505.1:n.299A=
ENST00000321612.6:c.2060A= ENSP00000370737.3:p.Lys687=
NM_000170.2:c.2060A= , LRG_643t1:c.2060A= NP_000161.2:p.Lys687=
NM_000170.3:c.2060A= MANE Select NP_000161.2:p.Lys687=