Canonical Allele Identifier: CA2580591268

Gene: GPX3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151021735T>G , CM000667.2:g.151021735T>G	GRCh38
NC_000005.9:g.150401296T>G , CM000667.1:g.150401296T>G	GRCh37
NC_000005.8:g.150381489T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002084.5:c.87+994T>G MANE Select	NP_002075.2:n.87+994T>G
ENST00000388825.9:c.87+994T>G MANE Select	ENSP00000373477.4:n.87+994T>G
NM_001329790.1:c.114+881T>G	NP_001316719.1:n.114+881T>G
NM_001329790.2:c.114+881T>G	NP_001316719.1:n.114+881T>G
NM_002084.3:c.87+994T>G	NP_002075.2:n.87+994T>G
NM_002084.4:c.87+994T>G	NP_002075.2:n.87+994T>G
ENST00000388825.8:c.87+994T>G	ENSP00000373477.4:n.87+994T>G
ENST00000517973.1:c.87+994T>G	ENSP00000429709.1:n.87+994T>G
ENST00000519214.5:c.*321+482T>G	ENSP00000430508.1:n.*321+482T>G
ENST00000521650.5:c.114+881T>G	ENSP00000427873.1:n.114+881T>G
ENST00000521722.5:n.150+994T>G
ENST00000614343.4:c.87+994T>G	ENSP00000483660.1:n.87+994T>G
ENST00000622181.4:c.87+994T>G	ENSP00000484258.1:n.87+994T>G
ENST00000625178.1:n.299T>G