Canonical Allele Identifier: CA372881899
Gene: GLDC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6558606C>A , CM000671.2:g.6558606C>A GRCh38
NC_000009.11:g.6558606C>A , CM000671.1:g.6558606C>A GRCh37
NC_000009.10:g.6548606C>A NCBI36
NG_016397.1:g.92087G>T , LRG_643:g.92087G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2005G>T MANE Select ENSP00000370737.4:p.Glu669Ter
ENST00000460457.2:n.165G>T
ENST00000638233.1:n.440G>T
ENST00000638661.1:c.205G>T ENSP00000491369.1:p.Glu69Ter
ENST00000638694.1:n.192G>T
ENST00000639318.1:c.205G>T ENSP00000491932.1:p.Glu69Ter
ENST00000639364.1:n.1705G>T
ENST00000639443.1:n.1573G>T
ENST00000639954.1:n.1713G>T
ENST00000640208.1:c.205G>T ENSP00000491895.1:p.Glu69Ter
ENST00000640505.1:n.244G>T
ENST00000640592.1:n.1888G>T
ENST00000321612.6:c.2005G>T ENSP00000370737.3:p.Glu669Ter
ENST00000460457.1:n.144G>T
NM_000170.2:c.2005G>T , LRG_643t1:c.2005G>T NP_000161.2:p.Glu669Ter
NM_000170.3:c.2005G>T MANE Select NP_000161.2:p.Glu669Ter