Canonical Allele Identifier: CA1591210084

Gene: GPX3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028389_151028391delinsATG , CM000667.2:g.151028389_151028391delinsATG	GRCh38
NC_000005.9:g.150407950_150407952delinsATG , CM000667.1:g.150407950_150407952delinsATG	GRCh37
NC_000005.8:g.150388143_150388145delinsATG	NCBI36
NG_030590.1:g.64270_64272delinsCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000388825.9:c.*259_*261delinsATG MANE Select	ENSP00000373477.4:n.*259_*261delinsATG
ENST00000388825.8:c.*259_*261delinsATG	ENSP00000373477.4:n.*259_*261delinsATG
ENST00000521632.1:c.749_751delinsATG
ENST00000614343.4:c.*721_*723delinsATG	ENSP00000483660.1:n.*721_*723delinsATG
ENST00000622181.4:c.*259_*261delinsATG	ENSP00000484258.1:n.*259_*261delinsATG
NM_002084.3:c.*259_*261delinsATG	NP_002075.2:n.*259_*261delinsATG
NM_001329790.1:c.*259_*261delinsATG	NP_001316719.1:n.*259_*261delinsATG
NM_002084.4:c.*259_*261delinsATG	NP_002075.2:n.*259_*261delinsATG
NM_002084.5:c.*259_*261delinsATG MANE Select	NP_002075.2:n.*259_*261delinsATG
NM_001329790.2:c.*259_*261delinsATG	NP_001316719.1:n.*259_*261delinsATG