Canonical Allele Identifier: CA903713567

Gene: ALG3 EIF2B5

Linked Data

• dbSNP Id: rs1273166182
• gnomAD v3: 3-184248694-C-G
• gnomAD v4: 3-184248694-C-G
• MyVariant Identifiers: chr3:g.183966482C>G (hg19) ; chr3:g.184248694C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184248694C>G , CM000665.2:g.184248694C>G	GRCh38
NC_000003.11:g.183966482C>G , CM000665.1:g.183966482C>G	GRCh37
NC_000003.10:g.185449176C>G	NCBI36
NG_008924.2:g.5819G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397676.8:c.196+51G>C (ALG3) MANE Select	ENSP00000380793.3:n.196+51G>C
ENST00000397676.7:c.196+51G>C (ALG3)	ENSP00000380793.3:n.196+51G>C
ENST00000411922.5:c.196+51G>C (ALG3)	ENSP00000394917.1:n.196+51G>C
ENST00000414845.5:c.189+51G>C (ALG3)
ENST00000423996.5:c.159+88G>C (ALG3)	ENSP00000407011.1:n.159+88G>C
ENST00000444495.1:c.2106+103987C>G (EIF2B5)	ENSP00000409142.1:n.2106+103987C>G
ENST00000445626.6:c.52+532G>C (ALG3)	ENSP00000402744.2:n.52+532G>C
ENST00000446569.1:c.154+88G>C (ALG3)
ENST00000455059.5:c.76+296G>C (ALG3)	ENSP00000397613.1:n.76+296G>C
ENST00000461415.5:n.169+88G>C (ALG3)
ENST00000482048.1:n.185+51G>C (ALG3)
ENST00000488976.5:n.181+88G>C (ALG3)
NM_001006941.2:c.52+532G>C (ALG3)	NP_001006942.1:n.52+532G>C
NM_005787.5:c.196+51G>C (ALG3)	NP_005778.1:n.196+51G>C
NR_024533.1:n.227+51G>C (ALG3)
NR_024534.1:n.190+88G>C (ALG3)
XM_011512323.1:c.76+296G>C (ALG3)	XP_011510625.1:n.76+296G>C
XM_011512323.2:c.76+296G>C (ALG3)	XP_011510625.1:n.76+296G>C
XM_024453296.1:c.-26-2882G>C (ALG3)	XP_024309064.1:n.-26-2882G>C
NM_005787.6:c.196+51G>C (ALG3) MANE Select	NP_005778.1:n.196+51G>C