Canonical Allele Identifier: CA1425931044

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245171G= , CM000665.2:g.184245171G=	GRCh38
NC_000003.11:g.183962959G= , CM000665.1:g.183962959G=	GRCh37
NC_000003.10:g.185445653G=	NCBI36
NG_008924.2:g.9342C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.605+27C= (ALG3) MANE Select	ENSP00000380793.3:n.605+27C=
ENST00000397676.7:c.605+27C= (ALG3)	ENSP00000380793.3:n.605+27C=
ENST00000411922.5:c.*181+27C= (ALG3)	ENSP00000394917.1:n.*181+27C=
ENST00000414845.5:c.337+297C= (ALG3)
ENST00000423996.5:c.*370+27C= (ALG3)	ENSP00000407011.1:n.*370+27C=
ENST00000444495.1:c.2106+100464G= (EIF2B5)	ENSP00000409142.1:n.2106+100464G=
ENST00000445626.6:c.461+27C= (ALG3)	ENSP00000402744.2:n.461+27C=
ENST00000446569.1:c.315+27C= (ALG3)
ENST00000455059.5:c.485+27C= (ALG3)	ENSP00000397613.1:n.485+27C=
ENST00000461415.5:n.605C= (ALG3)
ENST00000477959.1:n.145+27C= (ALG3)
ENST00000482048.1:n.621C= (ALG3)
ENST00000488976.5:n.517C= (ALG3)
NM_001006941.2:c.461+27C= (ALG3)	NP_001006942.1:n.461+27C=
NM_005787.5:c.605+27C= (ALG3)	NP_005778.1:n.605+27C=
NR_024533.1:n.536+27C= (ALG3)
NR_024534.1:n.599+27C= (ALG3)
XM_011512322.1:c.506+27C= (ALG3)	XP_011510624.1:n.506+27C=
XM_011512323.1:c.485+27C= (ALG3)	XP_011510625.1:n.485+27C=
XM_011512323.2:c.485+27C= (ALG3)	XP_011510625.1:n.485+27C=
XM_024453296.1:c.383+27C= (ALG3)	XP_024309064.1:n.383+27C=
NM_005787.6:c.605+27C= (ALG3) MANE Select	NP_005778.1:n.605+27C=