Canonical Allele Identifier: CA383181105

Gene: STT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.125597107A>G , CM000673.2:g.125597107A>G	GRCh38
NC_000011.9:g.125467002A>G , CM000673.1:g.125467002A>G	GRCh37
NC_000011.8:g.124972212A>G	NCBI36
NG_042806.1:g.9313A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_152713.5:c.137A>G MANE Select	NP_689926.1:p.His46Arg
ENST00000392708.9:c.137A>G MANE Select	ENSP00000376472.3:p.His46Arg
NM_001278503.1:c.137A>G	NP_001265432.1:p.His46Arg
NM_001278503.2:c.137A>G	NP_001265432.1:p.His46Arg
NM_001278504.1:c.-140A>G	NP_001265433.1:n.-140A>G
NM_001278504.2:c.-140A>G	NP_001265433.1:n.-140A>G
NM_152713.4:c.137A>G	NP_689926.1:p.His46Arg
ENST00000392708.8:c.137A>G	ENSP00000376472.3:p.His46Arg
ENST00000525652.5:c.137A>G	ENSP00000435810.1:p.His46Arg
ENST00000527606.5:c.137A>G	ENSP00000436558.1:p.His46Arg
ENST00000529196.5:c.137A>G	ENSP00000436962.1:p.His46Arg
ENST00000529886.1:c.137A>G	ENSP00000432912.1:p.His46Arg
ENST00000531491.5:c.-140A>G	ENSP00000432820.1:n.-140A>G
ENST00000534472.5:n.272A>G
ENST00000649491.1:c.137A>G	ENSP00000497336.1:p.His46Arg
XM_011542807.1:c.137A>G	XP_011541109.1:p.His46Arg
XM_011542807.3:c.137A>G	XP_011541109.1:p.His46Arg
XM_011542808.1:c.137A>G	XP_011541110.1:p.His46Arg
XR_001747860.2:n.244A>G