Canonical Allele Identifier: CA437327342

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963099G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245311G>T , CM000665.2:g.184245311G>T	GRCh38
NC_000003.11:g.183963099G>T , CM000665.1:g.183963099G>T	GRCh37
NC_000003.10:g.185445793G>T	NCBI36
NG_008924.2:g.9202C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.492C>A (ALG3) MANE Select	ENSP00000380793.3:p.Val164=
ENST00000397676.7:c.492C>A (ALG3)	ENSP00000380793.3:p.Val164=
ENST00000411922.5:c.*68C>A (ALG3)	ENSP00000394917.1:n.*68C>A
ENST00000414845.5:c.337+157C>A (ALG3)
ENST00000423996.5:c.*257C>A (ALG3)	ENSP00000407011.1:n.*257C>A
ENST00000444495.1:c.2106+100604G>T (EIF2B5)	ENSP00000409142.1:n.2106+100604G>T
ENST00000445626.6:c.348C>A (ALG3)	ENSP00000402744.2:p.Val116=
ENST00000446569.1:c.202C>A (ALG3)
ENST00000455059.5:c.372C>A (ALG3)	ENSP00000397613.1:p.Val124=
ENST00000461415.5:n.465C>A (ALG3)
ENST00000477959.1:n.32C>A (ALG3)
ENST00000482048.1:n.481C>A (ALG3)
ENST00000488976.5:n.377C>A (ALG3)
NM_001006941.2:c.348C>A (ALG3)	NP_001006942.1:p.Val116=
NM_005787.5:c.492C>A (ALG3)	NP_005778.1:p.Val164=
NR_024533.1:n.423C>A (ALG3)
NR_024534.1:n.486C>A (ALG3)
XM_011512322.1:c.393C>A (ALG3)	XP_011510624.1:p.Val131=
XM_011512323.1:c.372C>A (ALG3)	XP_011510625.1:p.Val124=
XM_011512323.2:c.372C>A (ALG3)	XP_011510625.1:p.Val124=
XM_024453296.1:c.270C>A (ALG3)	XP_024309064.1:p.Val90=
NM_005787.6:c.492C>A (ALG3) MANE Select	NP_005778.1:p.Val164=