Canonical Allele Identifier: CA1830527761
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6595012A= , CM000671.2:g.6595012A= GRCh38
NC_000009.11:g.6595012A= , CM000671.1:g.6595012A= GRCh37
NC_000009.10:g.6585012A= NCBI36
NG_016397.1:g.55681T= , LRG_643:g.55681T=

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.1261+2T= MANE Select ENSP00000370737.4:n.1261+2T=
ENST00000639364.1:n.961+2T=
ENST00000639443.1:n.829+2T=
ENST00000639493.1:n.413+2T=
ENST00000639954.1:n.969+2T=
ENST00000640592.1:n.1144+2T=
ENST00000321612.6:c.1261+2T= ENSP00000370737.3:n.1261+2T=
ENST00000463305.1:n.345+2T=
NM_000170.2:c.1261+2T= , LRG_643t1:c.1261+2T= NP_000161.2:n.1261+2T=
NM_000170.3:c.1261+2T= MANE Select NP_000161.2:n.1261+2T=