Canonical Allele Identifier: CA2676036230

Gene: GPX3

Linked Data

• gnomAD v4: 5-151028396-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028396T>A , CM000667.2:g.151028396T>A	GRCh38
NC_000005.9:g.150407957T>A , CM000667.1:g.150407957T>A	GRCh37
NC_000005.8:g.150388150T>A	NCBI36
NG_030590.1:g.64265A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388825.9:c.*266T>A MANE Select	ENSP00000373477.4:n.*266T>A
ENST00000388825.8:c.*266T>A	ENSP00000373477.4:n.*266T>A
ENST00000521632.1:c.756T>A
ENST00000614343.4:c.*728T>A	ENSP00000483660.1:n.*728T>A
ENST00000622181.4:c.*266T>A	ENSP00000484258.1:n.*266T>A
NM_002084.3:c.*266T>A	NP_002075.2:n.*266T>A
NM_001329790.1:c.*266T>A	NP_001316719.1:n.*266T>A
NM_002084.4:c.*266T>A	NP_002075.2:n.*266T>A
NM_002084.5:c.*266T>A MANE Select	NP_002075.2:n.*266T>A
NM_001329790.2:c.*266T>A	NP_001316719.1:n.*266T>A