Canonical Allele Identifier: CA2676036229

Gene: GPX3

Linked Data

• gnomAD v4: 5-151028395-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028395C>T , CM000667.2:g.151028395C>T	GRCh38
NC_000005.9:g.150407956C>T , CM000667.1:g.150407956C>T	GRCh37
NC_000005.8:g.150388149C>T	NCBI36
NG_030590.1:g.64266G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000388825.9:c.*265C>T MANE Select	ENSP00000373477.4:n.*265C>T
ENST00000388825.8:c.*265C>T	ENSP00000373477.4:n.*265C>T
ENST00000521632.1:c.755C>T
ENST00000614343.4:c.*727C>T	ENSP00000483660.1:n.*727C>T
ENST00000622181.4:c.*265C>T	ENSP00000484258.1:n.*265C>T
NM_002084.3:c.*265C>T	NP_002075.2:n.*265C>T
NM_001329790.1:c.*265C>T	NP_001316719.1:n.*265C>T
NM_002084.4:c.*265C>T	NP_002075.2:n.*265C>T
NM_002084.5:c.*265C>T MANE Select	NP_002075.2:n.*265C>T
NM_001329790.2:c.*265C>T	NP_001316719.1:n.*265C>T