Canonical Allele Identifier: CA865903489

Gene: GLDC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556839C>T , CM000671.2:g.6556839C>T	GRCh38
NC_000009.11:g.6556839C>T , CM000671.1:g.6556839C>T	GRCh37
NC_000009.10:g.6546839C>T	NCBI36
NG_016397.1:g.93854G>A , LRG_643:g.93854G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2053-537G>A MANE Select	ENSP00000370737.4:n.2053-537G>A
ENST00000638233.1:n.488-537G>A
ENST00000638661.1:c.253-537G>A	ENSP00000491369.1:n.253-537G>A
ENST00000638694.1:n.240-537G>A
ENST00000639318.1:c.253-537G>A	ENSP00000491932.1:n.253-537G>A
ENST00000639364.1:n.1753-537G>A
ENST00000639443.1:n.1621-537G>A
ENST00000639954.1:n.1761-537G>A
ENST00000640505.1:n.292-537G>A
ENST00000321612.6:c.2053-537G>A	ENSP00000370737.3:n.2053-537G>A
NM_000170.2:c.2053-537G>A , LRG_643t1:c.2053-537G>A	NP_000161.2:n.2053-537G>A
NM_000170.3:c.2053-537G>A MANE Select	NP_000161.2:n.2053-537G>A