Canonical Allele Identifier: CA437327369

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963310C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245522C>G , CM000665.2:g.184245522C>G	GRCh38
NC_000003.11:g.183963310C>G , CM000665.1:g.183963310C>G	GRCh37
NC_000003.10:g.185446004C>G	NCBI36
NG_008924.2:g.8991G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397676.8:c.390G>C (ALG3) MANE Select	ENSP00000380793.3:p.Val130=
ENST00000397676.7:c.390G>C (ALG3)	ENSP00000380793.3:p.Val130=
ENST00000411922.5:c.290G>C (ALG3)	ENSP00000394917.1:p.Cys97Ser
ENST00000414845.5:c.283G>C (ALG3)
ENST00000423996.5:c.*155G>C (ALG3)	ENSP00000407011.1:n.*155G>C
ENST00000444495.1:c.2106+100815C>G (EIF2B5)	ENSP00000409142.1:n.2106+100815C>G
ENST00000445626.6:c.246G>C (ALG3)	ENSP00000402744.2:p.Val82=
ENST00000446569.1:c.155-164G>C (ALG3)
ENST00000455059.5:c.270G>C (ALG3)	ENSP00000397613.1:p.Val90=
ENST00000461415.5:n.363G>C (ALG3)
ENST00000482048.1:n.379G>C (ALG3)
ENST00000488976.5:n.275G>C (ALG3)
NM_001006941.2:c.246G>C (ALG3)	NP_001006942.1:p.Val82=
NM_005787.5:c.390G>C (ALG3)	NP_005778.1:p.Val130=
NR_024533.1:n.321G>C (ALG3)
NR_024534.1:n.384G>C (ALG3)
XM_011512322.1:c.291G>C (ALG3)	XP_011510624.1:p.Val97=
XM_011512323.1:c.270G>C (ALG3)	XP_011510625.1:p.Val90=
XM_011512323.2:c.270G>C (ALG3)	XP_011510625.1:p.Val90=
XM_024453296.1:c.168G>C (ALG3)	XP_024309064.1:p.Val56=
NM_005787.6:c.390G>C (ALG3) MANE Select	NP_005778.1:p.Val130=