Canonical Allele Identifier: CA2689358078

Gene: GLDC

Linked Data

• gnomAD v4: 9-6556373-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556373T>G , CM000671.2:g.6556373T>G	GRCh38
NC_000009.11:g.6556373T>G , CM000671.1:g.6556373T>G	GRCh37
NC_000009.10:g.6546373T>G	NCBI36
NG_016397.1:g.94320A>C , LRG_643:g.94320A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2053-71A>C MANE Select	ENSP00000370737.4:n.2053-71A>C
ENST00000638233.1:n.488-71A>C
ENST00000638661.1:c.253-71A>C	ENSP00000491369.1:n.253-71A>C
ENST00000638694.1:n.240-71A>C
ENST00000639318.1:c.253-71A>C	ENSP00000491932.1:n.253-71A>C
ENST00000639364.1:n.1753-71A>C
ENST00000639443.1:n.1621-71A>C
ENST00000639954.1:n.1761-71A>C
ENST00000640505.1:n.292-71A>C
ENST00000321612.6:c.2053-71A>C	ENSP00000370737.3:n.2053-71A>C
NM_000170.2:c.2053-71A>C , LRG_643t1:c.2053-71A>C	NP_000161.2:n.2053-71A>C
NM_000170.3:c.2053-71A>C MANE Select	NP_000161.2:n.2053-71A>C