Canonical Allele Identifier: CA1425931180

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245445T= , CM000665.2:g.184245445T=	GRCh38
NC_000003.11:g.183963233T= , CM000665.1:g.183963233T=	GRCh37
NC_000003.10:g.185445927T=	NCBI36
NG_008924.2:g.9068A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397676.8:c.444+23A= (ALG3) MANE Select	ENSP00000380793.3:n.444+23A=
ENST00000397676.7:c.444+23A= (ALG3)	ENSP00000380793.3:n.444+23A=
ENST00000411922.5:c.*20+23A= (ALG3)	ENSP00000394917.1:n.*20+23A=
ENST00000414845.5:c.337+23A= (ALG3)
ENST00000423996.5:c.*209+23A= (ALG3)	ENSP00000407011.1:n.*209+23A=
ENST00000444495.1:c.2106+100738T= (EIF2B5)	ENSP00000409142.1:n.2106+100738T=
ENST00000445626.6:c.300+23A= (ALG3)	ENSP00000402744.2:n.300+23A=
ENST00000446569.1:c.155-87A= (ALG3)
ENST00000455059.5:c.324+23A= (ALG3)	ENSP00000397613.1:n.324+23A=
ENST00000461415.5:n.417+23A= (ALG3)
ENST00000482048.1:n.433+23A= (ALG3)
ENST00000488976.5:n.329+23A= (ALG3)
NM_001006941.2:c.300+23A= (ALG3)	NP_001006942.1:n.300+23A=
NM_005787.5:c.444+23A= (ALG3)	NP_005778.1:n.444+23A=
NR_024533.1:n.375+23A= (ALG3)
NR_024534.1:n.438+23A= (ALG3)
XM_011512322.1:c.345+23A= (ALG3)	XP_011510624.1:n.345+23A=
XM_011512323.1:c.324+23A= (ALG3)	XP_011510625.1:n.324+23A=
XM_011512323.2:c.324+23A= (ALG3)	XP_011510625.1:n.324+23A=
XM_024453296.1:c.222+23A= (ALG3)	XP_024309064.1:n.222+23A=
NM_005787.6:c.444+23A= (ALG3) MANE Select	NP_005778.1:n.444+23A=