Canonical Allele Identifier: CA1425931233

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245559C= , CM000665.2:g.184245559C=	GRCh38
NC_000003.11:g.183963347C= , CM000665.1:g.183963347C=	GRCh37
NC_000003.10:g.185446041C=	NCBI36
NG_008924.2:g.8954G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005787.6:c.353G= (ALG3) MANE Select	NP_005778.1:p.Gly118=
ENST00000397676.8:c.353G= (ALG3) MANE Select	ENSP00000380793.3:p.Gly118=
NM_001006941.2:c.209G= (ALG3)	NP_001006942.1:p.Gly70=
NM_005787.5:c.353G= (ALG3)	NP_005778.1:p.Gly118=
NR_024533.1:n.284G= (ALG3)
NR_024534.1:n.347G= (ALG3)
ENST00000397676.7:c.353G= (ALG3)	ENSP00000380793.3:p.Gly118=
ENST00000411922.5:c.253G= (ALG3)	ENSP00000394917.1:p.Ala85=
ENST00000414845.5:c.246G= (ALG3)
ENST00000423996.5:c.*118G= (ALG3)	ENSP00000407011.1:n.*118G=
ENST00000444495.1:c.2106+100852C= (EIF2B5)	ENSP00000409142.1:n.2106+100852C=
ENST00000445626.6:c.209G= (ALG3)	ENSP00000402744.2:p.Gly70=
ENST00000446569.1:c.155-201G= (ALG3)
ENST00000455059.5:c.233G= (ALG3)	ENSP00000397613.1:p.Gly78=
ENST00000461415.5:n.326G= (ALG3)
ENST00000482048.1:n.342G= (ALG3)
ENST00000488976.5:n.238G= (ALG3)
XM_011512322.1:c.254G= (ALG3)	XP_011510624.1:p.Gly85=
XM_011512323.1:c.233G= (ALG3)	XP_011510625.1:p.Gly78=
XM_011512323.2:c.233G= (ALG3)	XP_011510625.1:p.Gly78=
XM_024453296.1:c.131G= (ALG3)	XP_024309064.1:p.Gly44=