Canonical Allele Identifier: CA355421659

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963305T>A (hg19) ; chr3:g.184245517T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245517T>A , CM000665.2:g.184245517T>A	GRCh38
NC_000003.11:g.183963305T>A , CM000665.1:g.183963305T>A	GRCh37
NC_000003.10:g.185445999T>A	NCBI36
NG_008924.2:g.8996A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000397676.8:c.395A>T (ALG3) MANE Select	ENSP00000380793.3:p.Tyr132Phe
ENST00000397676.7:c.395A>T (ALG3)	ENSP00000380793.3:p.Tyr132Phe
ENST00000411922.5:c.295A>T (ALG3)	ENSP00000394917.1:p.Thr99Ser
ENST00000414845.5:c.288A>T (ALG3)
ENST00000423996.5:c.*160A>T (ALG3)	ENSP00000407011.1:n.*160A>T
ENST00000444495.1:c.2106+100810T>A (EIF2B5)	ENSP00000409142.1:n.2106+100810T>A
ENST00000445626.6:c.251A>T (ALG3)	ENSP00000402744.2:p.Tyr84Phe
ENST00000446569.1:c.155-159A>T (ALG3)
ENST00000455059.5:c.275A>T (ALG3)	ENSP00000397613.1:p.Tyr92Phe
ENST00000461415.5:n.368A>T (ALG3)
ENST00000482048.1:n.384A>T (ALG3)
ENST00000488976.5:n.280A>T (ALG3)
NM_001006941.2:c.251A>T (ALG3)	NP_001006942.1:p.Tyr84Phe
NM_005787.5:c.395A>T (ALG3)	NP_005778.1:p.Tyr132Phe
NR_024533.1:n.326A>T (ALG3)
NR_024534.1:n.389A>T (ALG3)
XM_011512322.1:c.296A>T (ALG3)	XP_011510624.1:p.Tyr99Phe
XM_011512323.1:c.275A>T (ALG3)	XP_011510625.1:p.Tyr92Phe
XM_011512323.2:c.275A>T (ALG3)	XP_011510625.1:p.Tyr92Phe
XM_024453296.1:c.173A>T (ALG3)	XP_024309064.1:p.Tyr58Phe
NM_005787.6:c.395A>T (ALG3) MANE Select	NP_005778.1:p.Tyr132Phe