Canonical Allele Identifier: CA355421302

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963089A>G (hg19) ; chr3:g.184245301A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245301A>G , CM000665.2:g.184245301A>G	GRCh38
NC_000003.11:g.183963089A>G , CM000665.1:g.183963089A>G	GRCh37
NC_000003.10:g.185445783A>G	NCBI36
NG_008924.2:g.9212T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.502T>C (ALG3) MANE Select	ENSP00000380793.3:p.Phe168Leu
ENST00000397676.7:c.502T>C (ALG3)	ENSP00000380793.3:p.Phe168Leu
ENST00000411922.5:c.*78T>C (ALG3)	ENSP00000394917.1:n.*78T>C
ENST00000414845.5:c.337+167T>C (ALG3)
ENST00000423996.5:c.*267T>C (ALG3)	ENSP00000407011.1:n.*267T>C
ENST00000444495.1:c.2106+100594A>G (EIF2B5)	ENSP00000409142.1:n.2106+100594A>G
ENST00000445626.6:c.358T>C (ALG3)	ENSP00000402744.2:p.Phe120Leu
ENST00000446569.1:c.212T>C (ALG3)
ENST00000455059.5:c.382T>C (ALG3)	ENSP00000397613.1:p.Phe128Leu
ENST00000461415.5:n.475T>C (ALG3)
ENST00000477959.1:n.42T>C (ALG3)
ENST00000482048.1:n.491T>C (ALG3)
ENST00000488976.5:n.387T>C (ALG3)
NM_001006941.2:c.358T>C (ALG3)	NP_001006942.1:p.Phe120Leu
NM_005787.5:c.502T>C (ALG3)	NP_005778.1:p.Phe168Leu
NR_024533.1:n.433T>C (ALG3)
NR_024534.1:n.496T>C (ALG3)
XM_011512322.1:c.403T>C (ALG3)	XP_011510624.1:p.Phe135Leu
XM_011512323.1:c.382T>C (ALG3)	XP_011510625.1:p.Phe128Leu
XM_011512323.2:c.382T>C (ALG3)	XP_011510625.1:p.Phe128Leu
XM_024453296.1:c.280T>C (ALG3)	XP_024309064.1:p.Phe94Leu
NM_005787.6:c.502T>C (ALG3) MANE Select	NP_005778.1:p.Phe168Leu