Canonical Allele Identifier: CA355421388

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963116A>G (hg19) ; chr3:g.184245328A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245328A>G , CM000665.2:g.184245328A>G	GRCh38
NC_000003.11:g.183963116A>G , CM000665.1:g.183963116A>G	GRCh37
NC_000003.10:g.185445810A>G	NCBI36
NG_008924.2:g.9185T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.475T>C (ALG3) MANE Select	ENSP00000380793.3:p.Cys159Arg
ENST00000397676.7:c.475T>C (ALG3)	ENSP00000380793.3:p.Cys159Arg
ENST00000411922.5:c.*51T>C (ALG3)	ENSP00000394917.1:n.*51T>C
ENST00000414845.5:c.337+140T>C (ALG3)
ENST00000423996.5:c.*240T>C (ALG3)	ENSP00000407011.1:n.*240T>C
ENST00000444495.1:c.2106+100621A>G (EIF2B5)	ENSP00000409142.1:n.2106+100621A>G
ENST00000445626.6:c.331T>C (ALG3)	ENSP00000402744.2:p.Cys111Arg
ENST00000446569.1:c.185T>C (ALG3)
ENST00000455059.5:c.355T>C (ALG3)	ENSP00000397613.1:p.Cys119Arg
ENST00000461415.5:n.448T>C (ALG3)
ENST00000477959.1:n.15T>C (ALG3)
ENST00000482048.1:n.464T>C (ALG3)
ENST00000488976.5:n.360T>C (ALG3)
NM_001006941.2:c.331T>C (ALG3)	NP_001006942.1:p.Cys111Arg
NM_005787.5:c.475T>C (ALG3)	NP_005778.1:p.Cys159Arg
NR_024533.1:n.406T>C (ALG3)
NR_024534.1:n.469T>C (ALG3)
XM_011512322.1:c.376T>C (ALG3)	XP_011510624.1:p.Cys126Arg
XM_011512323.1:c.355T>C (ALG3)	XP_011510625.1:p.Cys119Arg
XM_011512323.2:c.355T>C (ALG3)	XP_011510625.1:p.Cys119Arg
XM_024453296.1:c.253T>C (ALG3)	XP_024309064.1:p.Cys85Arg
NM_005787.6:c.475T>C (ALG3) MANE Select	NP_005778.1:p.Cys159Arg