Canonical Allele Identifier: CA355421258

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963074A>C (hg19) ; chr3:g.184245286A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245286A>C , CM000665.2:g.184245286A>C	GRCh38
NC_000003.11:g.183963074A>C , CM000665.1:g.183963074A>C	GRCh37
NC_000003.10:g.185445768A>C	NCBI36
NG_008924.2:g.9227T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.517T>G (ALG3) MANE Select	ENSP00000380793.3:p.Phe173Val
ENST00000397676.7:c.517T>G (ALG3)	ENSP00000380793.3:p.Phe173Val
ENST00000411922.5:c.*93T>G (ALG3)	ENSP00000394917.1:n.*93T>G
ENST00000414845.5:c.337+182T>G (ALG3)
ENST00000423996.5:c.*282T>G (ALG3)	ENSP00000407011.1:n.*282T>G
ENST00000444495.1:c.2106+100579A>C (EIF2B5)	ENSP00000409142.1:n.2106+100579A>C
ENST00000445626.6:c.373T>G (ALG3)	ENSP00000402744.2:p.Phe125Val
ENST00000446569.1:c.227T>G (ALG3)
ENST00000455059.5:c.397T>G (ALG3)	ENSP00000397613.1:p.Phe133Val
ENST00000461415.5:n.490T>G (ALG3)
ENST00000477959.1:n.57T>G (ALG3)
ENST00000482048.1:n.506T>G (ALG3)
ENST00000488976.5:n.402T>G (ALG3)
NM_001006941.2:c.373T>G (ALG3)	NP_001006942.1:p.Phe125Val
NM_005787.5:c.517T>G (ALG3)	NP_005778.1:p.Phe173Val
NR_024533.1:n.448T>G (ALG3)
NR_024534.1:n.511T>G (ALG3)
XM_011512322.1:c.418T>G (ALG3)	XP_011510624.1:p.Phe140Val
XM_011512323.1:c.397T>G (ALG3)	XP_011510625.1:p.Phe133Val
XM_011512323.2:c.397T>G (ALG3)	XP_011510625.1:p.Phe133Val
XM_024453296.1:c.295T>G (ALG3)	XP_024309064.1:p.Phe99Val
NM_005787.6:c.517T>G (ALG3) MANE Select	NP_005778.1:p.Phe173Val