Canonical Allele Identifier: CA1425931068

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245217A= , CM000665.2:g.184245217A=	GRCh38
NC_000003.11:g.183963005A= , CM000665.1:g.183963005A=	GRCh37
NC_000003.10:g.185445699A=	NCBI36
NG_008924.2:g.9296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.586T= (ALG3) MANE Select	ENSP00000380793.3:p.Trp196=
ENST00000397676.7:c.586T= (ALG3)	ENSP00000380793.3:p.Trp196=
ENST00000411922.5:c.*162T= (ALG3)	ENSP00000394917.1:n.*162T=
ENST00000414845.5:c.337+251T= (ALG3)
ENST00000423996.5:c.*351T= (ALG3)	ENSP00000407011.1:n.*351T=
ENST00000444495.1:c.2106+100510A= (EIF2B5)	ENSP00000409142.1:n.2106+100510A=
ENST00000445626.6:c.442T= (ALG3)	ENSP00000402744.2:p.Trp148=
ENST00000446569.1:c.296T= (ALG3)
ENST00000455059.5:c.466T= (ALG3)	ENSP00000397613.1:p.Trp156=
ENST00000461415.5:n.559T= (ALG3)
ENST00000477959.1:n.126T= (ALG3)
ENST00000482048.1:n.575T= (ALG3)
ENST00000488976.5:n.471T= (ALG3)
NM_001006941.2:c.442T= (ALG3)	NP_001006942.1:p.Trp148=
NM_005787.5:c.586T= (ALG3)	NP_005778.1:p.Trp196=
NR_024533.1:n.517T= (ALG3)
NR_024534.1:n.580T= (ALG3)
XM_011512322.1:c.487T= (ALG3)	XP_011510624.1:p.Trp163=
XM_011512323.1:c.466T= (ALG3)	XP_011510625.1:p.Trp156=
XM_011512323.2:c.466T= (ALG3)	XP_011510625.1:p.Trp156=
XM_024453296.1:c.364T= (ALG3)	XP_024309064.1:p.Trp122=
NM_005787.6:c.586T= (ALG3) MANE Select	NP_005778.1:p.Trp196=