Canonical Allele Identifier: CA1830469935
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6534681T= , CM000671.2:g.6534681T= GRCh38
NC_000009.11:g.6534681T= , CM000671.1:g.6534681T= GRCh37
NC_000009.10:g.6524681T= NCBI36
NG_016397.1:g.116012A= , LRG_643:g.116012A=

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.2919+27A= MANE Select ENSP00000370737.4:n.2919+27A=
ENST00000638233.1:n.1354+27A=
ENST00000638274.1:c.71+27A=
ENST00000638661.1:c.1119+27A= ENSP00000491369.1:n.1119+27A=
ENST00000638694.1:n.1106+27A=
ENST00000639318.1:c.1023+27A= ENSP00000491932.1:n.1023+27A=
ENST00000639364.1:n.2619+27A=
ENST00000639443.1:n.2487+27A=
ENST00000639461.1:n.2020+27A=
ENST00000639639.1:c.621+27A= ENSP00000491312.1:n.621+27A=
ENST00000639954.1:n.2627+27A=
ENST00000640505.1:n.1158+27A=
ENST00000321612.6:c.2919+27A= ENSP00000370737.3:n.2919+27A=
ENST00000477960.1:n.500+27A=
NM_000170.2:c.2919+27A= , LRG_643t1:c.2919+27A= NP_000161.2:n.2919+27A=
NM_000170.3:c.2919+27A= MANE Select NP_000161.2:n.2919+27A=