Canonical Allele Identifier: CA355421666

Gene: ALG3 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183963306A>T (hg19) ; chr3:g.184245518A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184245518A>T , CM000665.2:g.184245518A>T	GRCh38
NC_000003.11:g.183963306A>T , CM000665.1:g.183963306A>T	GRCh37
NC_000003.10:g.185446000A>T	NCBI36
NG_008924.2:g.8995T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000397676.8:c.394T>A (ALG3) MANE Select	ENSP00000380793.3:p.Tyr132Asn
ENST00000397676.7:c.394T>A (ALG3)	ENSP00000380793.3:p.Tyr132Asn
ENST00000411922.5:c.294T>A (ALG3)	ENSP00000394917.1:p.Ser98=
ENST00000414845.5:c.287T>A (ALG3)
ENST00000423996.5:c.*159T>A (ALG3)	ENSP00000407011.1:n.*159T>A
ENST00000444495.1:c.2106+100811A>T (EIF2B5)	ENSP00000409142.1:n.2106+100811A>T
ENST00000445626.6:c.250T>A (ALG3)	ENSP00000402744.2:p.Tyr84Asn
ENST00000446569.1:c.155-160T>A (ALG3)
ENST00000455059.5:c.274T>A (ALG3)	ENSP00000397613.1:p.Tyr92Asn
ENST00000461415.5:n.367T>A (ALG3)
ENST00000482048.1:n.383T>A (ALG3)
ENST00000488976.5:n.279T>A (ALG3)
NM_001006941.2:c.250T>A (ALG3)	NP_001006942.1:p.Tyr84Asn
NM_005787.5:c.394T>A (ALG3)	NP_005778.1:p.Tyr132Asn
NR_024533.1:n.325T>A (ALG3)
NR_024534.1:n.388T>A (ALG3)
XM_011512322.1:c.295T>A (ALG3)	XP_011510624.1:p.Tyr99Asn
XM_011512323.1:c.274T>A (ALG3)	XP_011510625.1:p.Tyr92Asn
XM_011512323.2:c.274T>A (ALG3)	XP_011510625.1:p.Tyr92Asn
XM_024453296.1:c.172T>A (ALG3)	XP_024309064.1:p.Tyr58Asn
NM_005787.6:c.394T>A (ALG3) MANE Select	NP_005778.1:p.Tyr132Asn