Canonical Allele Identifier: CA2676034722

Gene: GPX3

Linked Data

• gnomAD v4: 5-151026381-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151026381G>A , CM000667.2:g.151026381G>A	GRCh38
NC_000005.9:g.150405942G>A , CM000667.1:g.150405942G>A	GRCh37
NC_000005.8:g.150386135G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388825.9:c.242-519G>A MANE Select	ENSP00000373477.4:n.242-519G>A
ENST00000388825.8:c.242-519G>A	ENSP00000373477.4:n.242-519G>A
ENST00000517973.1:c.88-519G>A	ENSP00000429709.1:n.88-519G>A
ENST00000519214.5:c.*476-519G>A	ENSP00000430508.1:n.*476-519G>A
ENST00000521632.1:c.151-519G>A
ENST00000521650.5:c.269-519G>A	ENSP00000427873.1:n.269-519G>A
ENST00000521722.5:n.305-330G>A
ENST00000614343.4:c.*23-519G>A	ENSP00000483660.1:n.*23-519G>A
ENST00000622181.4:c.239-519G>A	ENSP00000484258.1:n.239-519G>A
NM_002084.3:c.242-519G>A	NP_002075.2:n.242-519G>A
NM_001329790.1:c.269-519G>A	NP_001316719.1:n.269-519G>A
NM_002084.4:c.242-519G>A	NP_002075.2:n.242-519G>A
NM_002084.5:c.242-519G>A MANE Select	NP_002075.2:n.242-519G>A
NM_001329790.2:c.269-519G>A	NP_001316719.1:n.269-519G>A