Canonical Allele Identifier: CA355420847

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183962990A>T (hg19) ; chr3:g.184245202A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245202A>T , CM000665.2:g.184245202A>T	GRCh38
NC_000003.11:g.183962990A>T , CM000665.1:g.183962990A>T	GRCh37
NC_000003.10:g.185445684A>T	NCBI36
NG_008924.2:g.9311T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.601T>A (ALG3) MANE Select	ENSP00000380793.3:p.Phe201Ile
ENST00000397676.7:c.601T>A (ALG3)	ENSP00000380793.3:p.Phe201Ile
ENST00000411922.5:c.*177T>A (ALG3)	ENSP00000394917.1:n.*177T>A
ENST00000414845.5:c.337+266T>A (ALG3)
ENST00000423996.5:c.*366T>A (ALG3)	ENSP00000407011.1:n.*366T>A
ENST00000444495.1:c.2106+100495A>T (EIF2B5)	ENSP00000409142.1:n.2106+100495A>T
ENST00000445626.6:c.457T>A (ALG3)	ENSP00000402744.2:p.Phe153Ile
ENST00000446569.1:c.311T>A (ALG3)
ENST00000455059.5:c.481T>A (ALG3)	ENSP00000397613.1:p.Phe161Ile
ENST00000461415.5:n.574T>A (ALG3)
ENST00000477959.1:n.141T>A (ALG3)
ENST00000482048.1:n.590T>A (ALG3)
ENST00000488976.5:n.486T>A (ALG3)
NM_001006941.2:c.457T>A (ALG3)	NP_001006942.1:p.Phe153Ile
NM_005787.5:c.601T>A (ALG3)	NP_005778.1:p.Phe201Ile
NR_024533.1:n.532T>A (ALG3)
NR_024534.1:n.595T>A (ALG3)
XM_011512322.1:c.502T>A (ALG3)	XP_011510624.1:p.Phe168Ile
XM_011512323.1:c.481T>A (ALG3)	XP_011510625.1:p.Phe161Ile
XM_011512323.2:c.481T>A (ALG3)	XP_011510625.1:p.Phe161Ile
XM_024453296.1:c.379T>A (ALG3)	XP_024309064.1:p.Phe127Ile
NM_005787.6:c.601T>A (ALG3) MANE Select	NP_005778.1:p.Phe201Ile