Canonical Allele Identifier: CA1425931145

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245378A= , CM000665.2:g.184245378A=	GRCh38
NC_000003.11:g.183963166A= , CM000665.1:g.183963166A=	GRCh37
NC_000003.10:g.185445860A=	NCBI36
NG_008924.2:g.9135T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.445-20T= (ALG3) MANE Select	ENSP00000380793.3:n.445-20T=
ENST00000397676.7:c.445-20T= (ALG3)	ENSP00000380793.3:n.445-20T=
ENST00000411922.5:c.*21-20T= (ALG3)	ENSP00000394917.1:n.*21-20T=
ENST00000414845.5:c.337+90T= (ALG3)
ENST00000423996.5:c.*210-20T= (ALG3)	ENSP00000407011.1:n.*210-20T=
ENST00000444495.1:c.2106+100671A= (EIF2B5)	ENSP00000409142.1:n.2106+100671A=
ENST00000445626.6:c.301-20T= (ALG3)	ENSP00000402744.2:n.301-20T=
ENST00000446569.1:c.155-20T= (ALG3)
ENST00000455059.5:c.325-20T= (ALG3)	ENSP00000397613.1:n.325-20T=
ENST00000461415.5:n.418-20T= (ALG3)
ENST00000482048.1:n.434-20T= (ALG3)
ENST00000488976.5:n.330-20T= (ALG3)
NM_001006941.2:c.301-20T= (ALG3)	NP_001006942.1:n.301-20T=
NM_005787.5:c.445-20T= (ALG3)	NP_005778.1:n.445-20T=
NR_024533.1:n.376-20T= (ALG3)
NR_024534.1:n.439-20T= (ALG3)
XM_011512322.1:c.346-20T= (ALG3)	XP_011510624.1:n.346-20T=
XM_011512323.1:c.325-20T= (ALG3)	XP_011510625.1:n.325-20T=
XM_011512323.2:c.325-20T= (ALG3)	XP_011510625.1:n.325-20T=
XM_024453296.1:c.223-20T= (ALG3)	XP_024309064.1:n.223-20T=
NM_005787.6:c.445-20T= (ALG3) MANE Select	NP_005778.1:n.445-20T=