Canonical Allele Identifier: CA1830493853
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556428T= , CM000671.2:g.6556428T= GRCh38
NC_000009.11:g.6556428T= , CM000671.1:g.6556428T= GRCh37
NC_000009.10:g.6546428T= NCBI36
NG_016397.1:g.94265A= , LRG_643:g.94265A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2053-126A= MANE Select ENSP00000370737.4:n.2053-126A=
ENST00000638233.1:n.488-126A=
ENST00000638661.1:c.253-126A= ENSP00000491369.1:n.253-126A=
ENST00000638694.1:n.240-126A=
ENST00000639318.1:c.253-126A= ENSP00000491932.1:n.253-126A=
ENST00000639364.1:n.1753-126A=
ENST00000639443.1:n.1621-126A=
ENST00000639954.1:n.1761-126A=
ENST00000640505.1:n.292-126A=
ENST00000321612.6:c.2053-126A= ENSP00000370737.3:n.2053-126A=
NM_000170.2:c.2053-126A= , LRG_643t1:c.2053-126A= NP_000161.2:n.2053-126A=
NM_000170.3:c.2053-126A= MANE Select NP_000161.2:n.2053-126A=