Canonical Allele Identifier: CA1591209989
Gene: GPX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151028300G= , CM000667.2:g.151028300G= GRCh38
NC_000005.9:g.150407861G= , CM000667.1:g.150407861G= GRCh37
NC_000005.8:g.150388054G= NCBI36
NG_030590.1:g.64361C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000388825.9:c.*170G= MANE Select ENSP00000373477.4:n.*170G=
ENST00000388825.8:c.*170G= ENSP00000373477.4:n.*170G=
ENST00000521632.1:c.660G=
ENST00000614343.4:c.*632G= ENSP00000483660.1:n.*632G=
ENST00000622181.4:c.*170G= ENSP00000484258.1:n.*170G=
NM_002084.3:c.*170G= NP_002075.2:n.*170G=
NM_001329790.1:c.*170G= NP_001316719.1:n.*170G=
NM_002084.4:c.*170G= NP_002075.2:n.*170G=
NM_002084.5:c.*170G= MANE Select NP_002075.2:n.*170G=
NM_001329790.2:c.*170G= NP_001316719.1:n.*170G=