Canonical Allele Identifier: CA2668818267

Gene: ALG3 EIF2B5

Linked Data

• gnomAD v4: 3-184245029-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245029T>G , CM000665.2:g.184245029T>G	GRCh38
NC_000003.11:g.183962817T>G , CM000665.1:g.183962817T>G	GRCh37
NC_000003.10:g.185445511T>G	NCBI36
NG_008924.2:g.9484A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.605+169A>C (ALG3) MANE Select	ENSP00000380793.3:n.605+169A>C
ENST00000397676.7:c.605+169A>C (ALG3)	ENSP00000380793.3:n.605+169A>C
ENST00000411922.5:c.*181+169A>C (ALG3)	ENSP00000394917.1:n.*181+169A>C
ENST00000414845.5:c.338-308A>C (ALG3)
ENST00000423996.5:c.*370+169A>C (ALG3)	ENSP00000407011.1:n.*370+169A>C
ENST00000444495.1:c.2106+100322T>G (EIF2B5)	ENSP00000409142.1:n.2106+100322T>G
ENST00000445626.6:c.461+169A>C (ALG3)	ENSP00000402744.2:n.461+169A>C
ENST00000446569.1:c.315+169A>C (ALG3)
ENST00000455059.5:c.485+169A>C (ALG3)	ENSP00000397613.1:n.485+169A>C
ENST00000461415.5:n.747A>C (ALG3)
ENST00000477959.1:n.145+169A>C (ALG3)
ENST00000488976.5:n.659A>C (ALG3)
NM_001006941.2:c.461+169A>C (ALG3)	NP_001006942.1:n.461+169A>C
NM_005787.5:c.605+169A>C (ALG3)	NP_005778.1:n.605+169A>C
NR_024533.1:n.536+169A>C (ALG3)
NR_024534.1:n.599+169A>C (ALG3)
XM_011512322.1:c.506+169A>C (ALG3)	XP_011510624.1:n.506+169A>C
XM_011512323.1:c.485+169A>C (ALG3)	XP_011510625.1:n.485+169A>C
XM_011512323.2:c.485+169A>C (ALG3)	XP_011510625.1:n.485+169A>C
XM_024453296.1:c.383+169A>C (ALG3)	XP_024309064.1:n.383+169A>C
NM_005787.6:c.605+169A>C (ALG3) MANE Select	NP_005778.1:n.605+169A>C