Canonical Allele Identifier: CA355421037

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963019G>A (hg19) ; chr3:g.184245231G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245231G>A , CM000665.2:g.184245231G>A	GRCh38
NC_000003.11:g.183963019G>A , CM000665.1:g.183963019G>A	GRCh37
NC_000003.10:g.185445713G>A	NCBI36
NG_008924.2:g.9282C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.572C>T (ALG3) MANE Select	ENSP00000380793.3:p.Ala191Val
ENST00000397676.7:c.572C>T (ALG3)	ENSP00000380793.3:p.Ala191Val
ENST00000411922.5:c.*148C>T (ALG3)	ENSP00000394917.1:n.*148C>T
ENST00000414845.5:c.337+237C>T (ALG3)
ENST00000423996.5:c.*337C>T (ALG3)	ENSP00000407011.1:n.*337C>T
ENST00000444495.1:c.2106+100524G>A (EIF2B5)	ENSP00000409142.1:n.2106+100524G>A
ENST00000445626.6:c.428C>T (ALG3)	ENSP00000402744.2:p.Ala143Val
ENST00000446569.1:c.282C>T (ALG3)
ENST00000455059.5:c.452C>T (ALG3)	ENSP00000397613.1:p.Ala151Val
ENST00000461415.5:n.545C>T (ALG3)
ENST00000477959.1:n.112C>T (ALG3)
ENST00000482048.1:n.561C>T (ALG3)
ENST00000488976.5:n.457C>T (ALG3)
NM_001006941.2:c.428C>T (ALG3)	NP_001006942.1:p.Ala143Val
NM_005787.5:c.572C>T (ALG3)	NP_005778.1:p.Ala191Val
NR_024533.1:n.503C>T (ALG3)
NR_024534.1:n.566C>T (ALG3)
XM_011512322.1:c.473C>T (ALG3)	XP_011510624.1:p.Ala158Val
XM_011512323.1:c.452C>T (ALG3)	XP_011510625.1:p.Ala151Val
XM_011512323.2:c.452C>T (ALG3)	XP_011510625.1:p.Ala151Val
XM_024453296.1:c.350C>T (ALG3)	XP_024309064.1:p.Ala117Val
NM_005787.6:c.572C>T (ALG3) MANE Select	NP_005778.1:p.Ala191Val