Canonical Allele Identifier: CA437327378

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963132G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245344G>C , CM000665.2:g.184245344G>C	GRCh38
NC_000003.11:g.183963132G>C , CM000665.1:g.183963132G>C	GRCh37
NC_000003.10:g.185445826G>C	NCBI36
NG_008924.2:g.9169C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.459C>G (ALG3) MANE Select	ENSP00000380793.3:p.Val153=
ENST00000397676.7:c.459C>G (ALG3)	ENSP00000380793.3:p.Val153=
ENST00000411922.5:c.*35C>G (ALG3)	ENSP00000394917.1:n.*35C>G
ENST00000414845.5:c.337+124C>G (ALG3)
ENST00000423996.5:c.*224C>G (ALG3)	ENSP00000407011.1:n.*224C>G
ENST00000444495.1:c.2106+100637G>C (EIF2B5)	ENSP00000409142.1:n.2106+100637G>C
ENST00000445626.6:c.315C>G (ALG3)	ENSP00000402744.2:p.Val105=
ENST00000446569.1:c.169C>G (ALG3)
ENST00000455059.5:c.339C>G (ALG3)	ENSP00000397613.1:p.Val113=
ENST00000461415.5:n.432C>G (ALG3)
ENST00000482048.1:n.448C>G (ALG3)
ENST00000488976.5:n.344C>G (ALG3)
NM_001006941.2:c.315C>G (ALG3)	NP_001006942.1:p.Val105=
NM_005787.5:c.459C>G (ALG3)	NP_005778.1:p.Val153=
NR_024533.1:n.390C>G (ALG3)
NR_024534.1:n.453C>G (ALG3)
XM_011512322.1:c.360C>G (ALG3)	XP_011510624.1:p.Val120=
XM_011512323.1:c.339C>G (ALG3)	XP_011510625.1:p.Val113=
XM_011512323.2:c.339C>G (ALG3)	XP_011510625.1:p.Val113=
XM_024453296.1:c.237C>G (ALG3)	XP_024309064.1:p.Val79=
NM_005787.6:c.459C>G (ALG3) MANE Select	NP_005778.1:p.Val153=