Canonical Allele Identifier: CA355421339

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963100A>T (hg19) ; chr3:g.184245312A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245312A>T , CM000665.2:g.184245312A>T	GRCh38
NC_000003.11:g.183963100A>T , CM000665.1:g.183963100A>T	GRCh37
NC_000003.10:g.185445794A>T	NCBI36
NG_008924.2:g.9201T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.491T>A (ALG3) MANE Select	ENSP00000380793.3:p.Val164Asp
ENST00000397676.7:c.491T>A (ALG3)	ENSP00000380793.3:p.Val164Asp
ENST00000411922.5:c.*67T>A (ALG3)	ENSP00000394917.1:n.*67T>A
ENST00000414845.5:c.337+156T>A (ALG3)
ENST00000423996.5:c.*256T>A (ALG3)	ENSP00000407011.1:n.*256T>A
ENST00000444495.1:c.2106+100605A>T (EIF2B5)	ENSP00000409142.1:n.2106+100605A>T
ENST00000445626.6:c.347T>A (ALG3)	ENSP00000402744.2:p.Val116Asp
ENST00000446569.1:c.201T>A (ALG3)
ENST00000455059.5:c.371T>A (ALG3)	ENSP00000397613.1:p.Val124Asp
ENST00000461415.5:n.464T>A (ALG3)
ENST00000477959.1:n.31T>A (ALG3)
ENST00000482048.1:n.480T>A (ALG3)
ENST00000488976.5:n.376T>A (ALG3)
NM_001006941.2:c.347T>A (ALG3)	NP_001006942.1:p.Val116Asp
NM_005787.5:c.491T>A (ALG3)	NP_005778.1:p.Val164Asp
NR_024533.1:n.422T>A (ALG3)
NR_024534.1:n.485T>A (ALG3)
XM_011512322.1:c.392T>A (ALG3)	XP_011510624.1:p.Val131Asp
XM_011512323.1:c.371T>A (ALG3)	XP_011510625.1:p.Val124Asp
XM_011512323.2:c.371T>A (ALG3)	XP_011510625.1:p.Val124Asp
XM_024453296.1:c.269T>A (ALG3)	XP_024309064.1:p.Val90Asp
NM_005787.6:c.491T>A (ALG3) MANE Select	NP_005778.1:p.Val164Asp