Canonical Allele Identifier: CA2676034789

Gene: GPX3

Linked Data

• gnomAD v4: 5-151026432-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151026432_151026433insCT , CM000667.2:g.151026432_151026433insCT	GRCh38
NC_000005.9:g.150405993_150405994insCT , CM000667.1:g.150405993_150405994insCT	GRCh37
NC_000005.8:g.150386186_150386187insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388825.9:c.242-468_242-467insCT MANE Select	ENSP00000373477.4:n.242-468_242-467insCT
ENST00000388825.8:c.242-468_242-467insCT	ENSP00000373477.4:n.242-468_242-467insCT
ENST00000517973.1:c.88-468_88-467insCT	ENSP00000429709.1:n.88-468_88-467insCT
ENST00000519214.5:c.*476-468_*476-467insCT	ENSP00000430508.1:n.*476-468_*476-467insCT
ENST00000521632.1:c.151-468_151-467insCT
ENST00000521650.5:c.269-468_269-467insCT	ENSP00000427873.1:n.269-468_269-467insCT
ENST00000521722.5:n.305-279_305-278insCT
ENST00000614343.4:c.*23-468_*23-467insCT	ENSP00000483660.1:n.*23-468_*23-467insCT
ENST00000622181.4:c.239-468_239-467insCT	ENSP00000484258.1:n.239-468_239-467insCT
NM_002084.3:c.242-468_242-467insCT	NP_002075.2:n.242-468_242-467insCT
NM_001329790.1:c.269-468_269-467insCT	NP_001316719.1:n.269-468_269-467insCT
NM_002084.4:c.242-468_242-467insCT	NP_002075.2:n.242-468_242-467insCT
NM_002084.5:c.242-468_242-467insCT MANE Select	NP_002075.2:n.242-468_242-467insCT
NM_001329790.2:c.269-468_269-467insCT	NP_001316719.1:n.269-468_269-467insCT