Canonical Allele Identifier: CA2676035930

Gene: GPX3

Linked Data

• gnomAD v4: 5-151028279-C-T

Genomic Alleles

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

Transcript Alleles

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