Canonical Allele Identifier: CA355421085

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963028A>C (hg19) ; chr3:g.184245240A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245240A>C , CM000665.2:g.184245240A>C	GRCh38
NC_000003.11:g.183963028A>C , CM000665.1:g.183963028A>C	GRCh37
NC_000003.10:g.185445722A>C	NCBI36
NG_008924.2:g.9273T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.563T>G (ALG3) MANE Select	ENSP00000380793.3:p.Leu188Arg
ENST00000397676.7:c.563T>G (ALG3)	ENSP00000380793.3:p.Leu188Arg
ENST00000411922.5:c.*139T>G (ALG3)	ENSP00000394917.1:n.*139T>G
ENST00000414845.5:c.337+228T>G (ALG3)
ENST00000423996.5:c.*328T>G (ALG3)	ENSP00000407011.1:n.*328T>G
ENST00000444495.1:c.2106+100533A>C (EIF2B5)	ENSP00000409142.1:n.2106+100533A>C
ENST00000445626.6:c.419T>G (ALG3)	ENSP00000402744.2:p.Leu140Arg
ENST00000446569.1:c.273T>G (ALG3)
ENST00000455059.5:c.443T>G (ALG3)	ENSP00000397613.1:p.Leu148Arg
ENST00000461415.5:n.536T>G (ALG3)
ENST00000477959.1:n.103T>G (ALG3)
ENST00000482048.1:n.552T>G (ALG3)
ENST00000488976.5:n.448T>G (ALG3)
NM_001006941.2:c.419T>G (ALG3)	NP_001006942.1:p.Leu140Arg
NM_005787.5:c.563T>G (ALG3)	NP_005778.1:p.Leu188Arg
NR_024533.1:n.494T>G (ALG3)
NR_024534.1:n.557T>G (ALG3)
XM_011512322.1:c.464T>G (ALG3)	XP_011510624.1:p.Leu155Arg
XM_011512323.1:c.443T>G (ALG3)	XP_011510625.1:p.Leu148Arg
XM_011512323.2:c.443T>G (ALG3)	XP_011510625.1:p.Leu148Arg
XM_024453296.1:c.341T>G (ALG3)	XP_024309064.1:p.Leu114Arg
NM_005787.6:c.563T>G (ALG3) MANE Select	NP_005778.1:p.Leu188Arg