Canonical Allele Identifier: CA1425931129

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245339A= , CM000665.2:g.184245339A=	GRCh38
NC_000003.11:g.183963127A= , CM000665.1:g.183963127A=	GRCh37
NC_000003.10:g.185445821A=	NCBI36
NG_008924.2:g.9174T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.464T= (ALG3) MANE Select	ENSP00000380793.3:p.Phe155=
ENST00000397676.7:c.464T= (ALG3)	ENSP00000380793.3:p.Phe155=
ENST00000411922.5:c.*40T= (ALG3)	ENSP00000394917.1:n.*40T=
ENST00000414845.5:c.337+129T= (ALG3)
ENST00000423996.5:c.*229T= (ALG3)	ENSP00000407011.1:n.*229T=
ENST00000444495.1:c.2106+100632A= (EIF2B5)	ENSP00000409142.1:n.2106+100632A=
ENST00000445626.6:c.320T= (ALG3)	ENSP00000402744.2:p.Phe107=
ENST00000446569.1:c.174T= (ALG3)
ENST00000455059.5:c.344T= (ALG3)	ENSP00000397613.1:p.Phe115=
ENST00000461415.5:n.437T= (ALG3)
ENST00000477959.1:n.4T= (ALG3)
ENST00000482048.1:n.453T= (ALG3)
ENST00000488976.5:n.349T= (ALG3)
NM_001006941.2:c.320T= (ALG3)	NP_001006942.1:p.Phe107=
NM_005787.5:c.464T= (ALG3)	NP_005778.1:p.Phe155=
NR_024533.1:n.395T= (ALG3)
NR_024534.1:n.458T= (ALG3)
XM_011512322.1:c.365T= (ALG3)	XP_011510624.1:p.Phe122=
XM_011512323.1:c.344T= (ALG3)	XP_011510625.1:p.Phe115=
XM_011512323.2:c.344T= (ALG3)	XP_011510625.1:p.Phe115=
XM_024453296.1:c.242T= (ALG3)	XP_024309064.1:p.Phe81=
NM_005787.6:c.464T= (ALG3) MANE Select	NP_005778.1:p.Phe155=