Canonical Allele Identifier: CA1830493719

Gene: GLDC

Linked Data

• dbSNP Id: rs1817630665

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556321A>G , CM000671.2:g.6556321A>G	GRCh38
NC_000009.11:g.6556321A>G , CM000671.1:g.6556321A>G	GRCh37
NC_000009.10:g.6546321A>G	NCBI36
NG_016397.1:g.94372T>C , LRG_643:g.94372T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.2053-19T>C MANE Select	ENSP00000370737.4:n.2053-19T>C
ENST00000638233.1:n.488-19T>C
ENST00000638661.1:c.253-19T>C	ENSP00000491369.1:n.253-19T>C
ENST00000638694.1:n.240-19T>C
ENST00000639318.1:c.253-19T>C	ENSP00000491932.1:n.253-19T>C
ENST00000639364.1:n.1753-19T>C
ENST00000639443.1:n.1621-19T>C
ENST00000639954.1:n.1761-19T>C
ENST00000640505.1:n.292-19T>C
ENST00000321612.6:c.2053-19T>C	ENSP00000370737.3:n.2053-19T>C
NM_000170.2:c.2053-19T>C , LRG_643t1:c.2053-19T>C	NP_000161.2:n.2053-19T>C
NM_000170.3:c.2053-19T>C MANE Select	NP_000161.2:n.2053-19T>C