Canonical Allele Identifier: CA437327224

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963006G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245218G>C , CM000665.2:g.184245218G>C	GRCh38
NC_000003.11:g.183963006G>C , CM000665.1:g.183963006G>C	GRCh37
NC_000003.10:g.185445700G>C	NCBI36
NG_008924.2:g.9295C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.585C>G (ALG3) MANE Select	ENSP00000380793.3:p.Gly195=
ENST00000397676.7:c.585C>G (ALG3)	ENSP00000380793.3:p.Gly195=
ENST00000411922.5:c.*161C>G (ALG3)	ENSP00000394917.1:n.*161C>G
ENST00000414845.5:c.337+250C>G (ALG3)
ENST00000423996.5:c.*350C>G (ALG3)	ENSP00000407011.1:n.*350C>G
ENST00000444495.1:c.2106+100511G>C (EIF2B5)	ENSP00000409142.1:n.2106+100511G>C
ENST00000445626.6:c.441C>G (ALG3)	ENSP00000402744.2:p.Gly147=
ENST00000446569.1:c.295C>G (ALG3)
ENST00000455059.5:c.465C>G (ALG3)	ENSP00000397613.1:p.Gly155=
ENST00000461415.5:n.558C>G (ALG3)
ENST00000477959.1:n.125C>G (ALG3)
ENST00000482048.1:n.574C>G (ALG3)
ENST00000488976.5:n.470C>G (ALG3)
NM_001006941.2:c.441C>G (ALG3)	NP_001006942.1:p.Gly147=
NM_005787.5:c.585C>G (ALG3)	NP_005778.1:p.Gly195=
NR_024533.1:n.516C>G (ALG3)
NR_024534.1:n.579C>G (ALG3)
XM_011512322.1:c.486C>G (ALG3)	XP_011510624.1:p.Gly162=
XM_011512323.1:c.465C>G (ALG3)	XP_011510625.1:p.Gly155=
XM_011512323.2:c.465C>G (ALG3)	XP_011510625.1:p.Gly155=
XM_024453296.1:c.363C>G (ALG3)	XP_024309064.1:p.Gly121=
NM_005787.6:c.585C>G (ALG3) MANE Select	NP_005778.1:p.Gly195=