Canonical Allele Identifier: CA1425931067

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245213C= , CM000665.2:g.184245213C=	GRCh38
NC_000003.11:g.183963001C= , CM000665.1:g.183963001C=	GRCh37
NC_000003.10:g.185445695C=	NCBI36
NG_008924.2:g.9300G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.590G= (ALG3) MANE Select	ENSP00000380793.3:p.Gly197=
ENST00000397676.7:c.590G= (ALG3)	ENSP00000380793.3:p.Gly197=
ENST00000411922.5:c.*166G= (ALG3)	ENSP00000394917.1:n.*166G=
ENST00000414845.5:c.337+255G= (ALG3)
ENST00000423996.5:c.*355G= (ALG3)	ENSP00000407011.1:n.*355G=
ENST00000444495.1:c.2106+100506C= (EIF2B5)	ENSP00000409142.1:n.2106+100506C=
ENST00000445626.6:c.446G= (ALG3)	ENSP00000402744.2:p.Gly149=
ENST00000446569.1:c.300G= (ALG3)
ENST00000455059.5:c.470G= (ALG3)	ENSP00000397613.1:p.Gly157=
ENST00000461415.5:n.563G= (ALG3)
ENST00000477959.1:n.130G= (ALG3)
ENST00000482048.1:n.579G= (ALG3)
ENST00000488976.5:n.475G= (ALG3)
NM_001006941.2:c.446G= (ALG3)	NP_001006942.1:p.Gly149=
NM_005787.5:c.590G= (ALG3)	NP_005778.1:p.Gly197=
NR_024533.1:n.521G= (ALG3)
NR_024534.1:n.584G= (ALG3)
XM_011512322.1:c.491G= (ALG3)	XP_011510624.1:p.Gly164=
XM_011512323.1:c.470G= (ALG3)	XP_011510625.1:p.Gly157=
XM_011512323.2:c.470G= (ALG3)	XP_011510625.1:p.Gly157=
XM_024453296.1:c.368G= (ALG3)	XP_024309064.1:p.Gly123=
NM_005787.6:c.590G= (ALG3) MANE Select	NP_005778.1:p.Gly197=