Canonical Allele Identifier: CA1591207991
Gene: GPX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151026433_151026434delinsGA , CM000667.2:g.151026433_151026434delinsGA GRCh38
NC_000005.9:g.150405994_150405995delinsGA , CM000667.1:g.150405994_150405995delinsGA GRCh37
NC_000005.8:g.150386187_150386188delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388825.9:c.242-467_242-466delinsGA MANE Select ENSP00000373477.4:n.242-467_242-466delinsGA
ENST00000388825.8:c.242-467_242-466delinsGA ENSP00000373477.4:n.242-467_242-466delinsGA
ENST00000517973.1:c.88-467_88-466delinsGA ENSP00000429709.1:n.88-467_88-466delinsGA
ENST00000519214.5:c.*476-467_*476-466delinsGA ENSP00000430508.1:n.*476-467_*476-466delinsGA
ENST00000521632.1:c.151-467_151-466delinsGA
ENST00000521650.5:c.269-467_269-466delinsGA ENSP00000427873.1:n.269-467_269-466delinsGA
ENST00000521722.5:n.305-278_305-277delinsGA
ENST00000614343.4:c.*23-467_*23-466delinsGA ENSP00000483660.1:n.*23-467_*23-466delinsGA
ENST00000622181.4:c.239-467_239-466delinsGA ENSP00000484258.1:n.239-467_239-466delinsGA
NM_002084.3:c.242-467_242-466delinsGA NP_002075.2:n.242-467_242-466delinsGA
NM_001329790.1:c.269-467_269-466delinsGA NP_001316719.1:n.269-467_269-466delinsGA
NM_002084.4:c.242-467_242-466delinsGA NP_002075.2:n.242-467_242-466delinsGA
NM_002084.5:c.242-467_242-466delinsGA MANE Select NP_002075.2:n.242-467_242-466delinsGA
NM_001329790.2:c.269-467_269-466delinsGA NP_001316719.1:n.269-467_269-466delinsGA