Canonical Allele Identifier: CA355421699

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963317A>T (hg19) ; chr3:g.184245529A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245529A>T , CM000665.2:g.184245529A>T	GRCh38
NC_000003.11:g.183963317A>T , CM000665.1:g.183963317A>T	GRCh37
NC_000003.10:g.185446011A>T	NCBI36
NG_008924.2:g.8984T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000397676.8:c.383T>A (ALG3) MANE Select	ENSP00000380793.3:p.Phe128Tyr
ENST00000397676.7:c.383T>A (ALG3)	ENSP00000380793.3:p.Phe128Tyr
ENST00000411922.5:c.283T>A (ALG3)	ENSP00000394917.1:p.Leu95Met
ENST00000414845.5:c.276T>A (ALG3)
ENST00000423996.5:c.*148T>A (ALG3)	ENSP00000407011.1:n.*148T>A
ENST00000444495.1:c.2106+100822A>T (EIF2B5)	ENSP00000409142.1:n.2106+100822A>T
ENST00000445626.6:c.239T>A (ALG3)	ENSP00000402744.2:p.Phe80Tyr
ENST00000446569.1:c.155-171T>A (ALG3)
ENST00000455059.5:c.263T>A (ALG3)	ENSP00000397613.1:p.Phe88Tyr
ENST00000461415.5:n.356T>A (ALG3)
ENST00000482048.1:n.372T>A (ALG3)
ENST00000488976.5:n.268T>A (ALG3)
NM_001006941.2:c.239T>A (ALG3)	NP_001006942.1:p.Phe80Tyr
NM_005787.5:c.383T>A (ALG3)	NP_005778.1:p.Phe128Tyr
NR_024533.1:n.314T>A (ALG3)
NR_024534.1:n.377T>A (ALG3)
XM_011512322.1:c.284T>A (ALG3)	XP_011510624.1:p.Phe95Tyr
XM_011512323.1:c.263T>A (ALG3)	XP_011510625.1:p.Phe88Tyr
XM_011512323.2:c.263T>A (ALG3)	XP_011510625.1:p.Phe88Tyr
XM_024453296.1:c.161T>A (ALG3)	XP_024309064.1:p.Phe54Tyr
NM_005787.6:c.383T>A (ALG3) MANE Select	NP_005778.1:p.Phe128Tyr