Canonical Allele Identifier: CA1830479683
Community Standard Title: NM_000170.3(GLDC):c.2665+1G=
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6540050C= , CM000671.2:g.6540050C= GRCh38
NC_000009.11:g.6540050C= , CM000671.1:g.6540050C= GRCh37
NC_000009.10:g.6530050C= NCBI36
NG_016397.1:g.110643G= , LRG_643:g.110643G=

Transcript Alleles

HGVS Amino-acid Change
NM_000170.3:c.2665+1G= MANE Select NP_000161.2:n.2665+1G=
ENST00000321612.8:c.2665+1G= MANE Select ENSP00000370737.4:n.2665+1G=
NM_000170.2:c.2665+1G= , LRG_643t1:c.2665+1G= NP_000161.2:n.2665+1G=
ENST00000321612.6:c.2665+1G= ENSP00000370737.3:n.2665+1G=
ENST00000477960.1:n.129+1G=
ENST00000638233.1:n.1100+1G=
ENST00000638661.1:c.865+1G= ENSP00000491369.1:n.865+1G=
ENST00000638694.1:n.852+1G=
ENST00000639318.1:c.770-3814G= ENSP00000491932.1:n.770-3814G=
ENST00000639364.1:n.2365+1G=
ENST00000639443.1:n.2233+1G=
ENST00000639461.1:n.1766+1G=
ENST00000639639.1:c.367+1G= ENSP00000491312.1:n.367+1G=
ENST00000639954.1:n.2373+1G=
ENST00000640505.1:n.904+1G=