Canonical Allele Identifier: CA1830469940
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6534687A= , CM000671.2:g.6534687A= GRCh38
NC_000009.11:g.6534687A= , CM000671.1:g.6534687A= GRCh37
NC_000009.10:g.6524687A= NCBI36
NG_016397.1:g.116006T= , LRG_643:g.116006T=

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.2919+21T= MANE Select ENSP00000370737.4:n.2919+21T=
ENST00000638233.1:n.1354+21T=
ENST00000638274.1:c.71+21T=
ENST00000638661.1:c.1119+21T= ENSP00000491369.1:n.1119+21T=
ENST00000638694.1:n.1106+21T=
ENST00000639318.1:c.1023+21T= ENSP00000491932.1:n.1023+21T=
ENST00000639364.1:n.2619+21T=
ENST00000639443.1:n.2487+21T=
ENST00000639461.1:n.2020+21T=
ENST00000639639.1:c.621+21T= ENSP00000491312.1:n.621+21T=
ENST00000639954.1:n.2627+21T=
ENST00000640505.1:n.1158+21T=
ENST00000321612.6:c.2919+21T= ENSP00000370737.3:n.2919+21T=
ENST00000477960.1:n.500+21T=
NM_000170.2:c.2919+21T= , LRG_643t1:c.2919+21T= NP_000161.2:n.2919+21T=
NM_000170.3:c.2919+21T= MANE Select NP_000161.2:n.2919+21T=