Canonical Allele Identifier: CA2676035927

Gene: GPX3

Linked Data

• gnomAD v4: 5-151028279-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028279C>A , CM000667.2:g.151028279C>A	GRCh38
NC_000005.9:g.150407840C>A , CM000667.1:g.150407840C>A	GRCh37
NC_000005.8:g.150388033C>A	NCBI36
NG_030590.1:g.64382G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388825.9:c.*149C>A MANE Select	ENSP00000373477.4:n.*149C>A
ENST00000388825.8:c.*149C>A	ENSP00000373477.4:n.*149C>A
ENST00000521632.1:c.639C>A
ENST00000614343.4:c.*611C>A	ENSP00000483660.1:n.*611C>A
ENST00000622181.4:c.*149C>A	ENSP00000484258.1:n.*149C>A
NM_002084.3:c.*149C>A	NP_002075.2:n.*149C>A
NM_001329790.1:c.*149C>A	NP_001316719.1:n.*149C>A
NM_002084.4:c.*149C>A	NP_002075.2:n.*149C>A
NM_002084.5:c.*149C>A MANE Select	NP_002075.2:n.*149C>A
NM_001329790.2:c.*149C>A	NP_001316719.1:n.*149C>A