Canonical Allele Identifier: CA437327243

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963015C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245227C>T , CM000665.2:g.184245227C>T	GRCh38
NC_000003.11:g.183963015C>T , CM000665.1:g.183963015C>T	GRCh37
NC_000003.10:g.185445709C>T	NCBI36
NG_008924.2:g.9286G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.576G>A (ALG3) MANE Select	ENSP00000380793.3:p.Gln192=
ENST00000397676.7:c.576G>A (ALG3)	ENSP00000380793.3:p.Gln192=
ENST00000411922.5:c.*152G>A (ALG3)	ENSP00000394917.1:n.*152G>A
ENST00000414845.5:c.337+241G>A (ALG3)
ENST00000423996.5:c.*341G>A (ALG3)	ENSP00000407011.1:n.*341G>A
ENST00000444495.1:c.2106+100520C>T (EIF2B5)	ENSP00000409142.1:n.2106+100520C>T
ENST00000445626.6:c.432G>A (ALG3)	ENSP00000402744.2:p.Gln144=
ENST00000446569.1:c.286G>A (ALG3)
ENST00000455059.5:c.456G>A (ALG3)	ENSP00000397613.1:p.Gln152=
ENST00000461415.5:n.549G>A (ALG3)
ENST00000477959.1:n.116G>A (ALG3)
ENST00000482048.1:n.565G>A (ALG3)
ENST00000488976.5:n.461G>A (ALG3)
NM_001006941.2:c.432G>A (ALG3)	NP_001006942.1:p.Gln144=
NM_005787.5:c.576G>A (ALG3)	NP_005778.1:p.Gln192=
NR_024533.1:n.507G>A (ALG3)
NR_024534.1:n.570G>A (ALG3)
XM_011512322.1:c.477G>A (ALG3)	XP_011510624.1:p.Gln159=
XM_011512323.1:c.456G>A (ALG3)	XP_011510625.1:p.Gln152=
XM_011512323.2:c.456G>A (ALG3)	XP_011510625.1:p.Gln152=
XM_024453296.1:c.354G>A (ALG3)	XP_024309064.1:p.Gln118=
NM_005787.6:c.576G>A (ALG3) MANE Select	NP_005778.1:p.Gln192=