Canonical Allele Identifier: CA372881929
Gene: GLDC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558621T>A , CM000671.2:g.6558621T>A GRCh38
NC_000009.11:g.6558621T>A , CM000671.1:g.6558621T>A GRCh37
NC_000009.10:g.6548621T>A NCBI36
NG_016397.1:g.92072A>T , LRG_643:g.92072A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.1990A>T MANE Select ENSP00000370737.4:p.Lys664Ter
ENST00000460457.2:n.150A>T
ENST00000638233.1:n.425A>T
ENST00000638661.1:c.190A>T ENSP00000491369.1:p.Lys64Ter
ENST00000638694.1:n.177A>T
ENST00000639318.1:c.190A>T ENSP00000491932.1:p.Lys64Ter
ENST00000639364.1:n.1690A>T
ENST00000639443.1:n.1558A>T
ENST00000639954.1:n.1698A>T
ENST00000640208.1:c.190A>T ENSP00000491895.1:p.Lys64Ter
ENST00000640505.1:n.229A>T
ENST00000640592.1:n.1873A>T
ENST00000321612.6:c.1990A>T ENSP00000370737.3:p.Lys664Ter
ENST00000460457.1:n.129A>T
NM_000170.2:c.1990A>T , LRG_643t1:c.1990A>T NP_000161.2:p.Lys664Ter
NM_000170.3:c.1990A>T MANE Select NP_000161.2:p.Lys664Ter