Canonical Allele Identifier: CA355417568

Gene: ALG3 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184242643C>T , CM000665.2:g.184242643C>T	GRCh38
NC_000003.11:g.183960431C>T , CM000665.1:g.183960431C>T	GRCh37
NC_000003.10:g.185443125C>T	NCBI36
NG_008924.2:g.11870G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005787.6:c.1188G>A (ALG3) MANE Select	NP_005778.1:p.Trp396Ter
ENST00000397676.8:c.1188G>A (ALG3) MANE Select	ENSP00000380793.3:p.Trp396Ter
NM_001006941.2:c.1044G>A (ALG3)	NP_001006942.1:p.Trp348Ter
NM_005787.5:c.1188G>A (ALG3)	NP_005778.1:p.Trp396Ter
NR_024533.1:n.1119G>A (ALG3)
NR_024534.1:n.1182G>A (ALG3)
ENST00000397676.7:c.1188G>A (ALG3)	ENSP00000380793.3:p.Trp396Ter
ENST00000411922.5:c.*764G>A (ALG3)	ENSP00000394917.1:n.*764G>A
ENST00000444495.1:c.2106+97936C>T (EIF2B5)	ENSP00000409142.1:n.2106+97936C>T
ENST00000445626.6:c.1044G>A (ALG3)	ENSP00000402744.2:p.Trp348Ter
ENST00000446569.1:c.898G>A (ALG3)
ENST00000455059.5:c.1068G>A (ALG3)	ENSP00000397613.1:p.Trp356Ter
ENST00000485912.1:n.811G>A (ALG3)
XM_011512322.1:c.1089G>A (ALG3)	XP_011510624.1:p.Trp363Ter
XM_011512323.1:c.1068G>A (ALG3)	XP_011510625.1:p.Trp356Ter
XM_011512323.2:c.1068G>A (ALG3)	XP_011510625.1:p.Trp356Ter
XM_024453296.1:c.966G>A (ALG3)	XP_024309064.1:p.Trp322Ter