Canonical Allele Identifier: CA2676035951

Gene: GPX3

Linked Data

• gnomAD v4: 5-151028291-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028291A>T , CM000667.2:g.151028291A>T	GRCh38
NC_000005.9:g.150407852A>T , CM000667.1:g.150407852A>T	GRCh37
NC_000005.8:g.150388045A>T	NCBI36
NG_030590.1:g.64370T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000388825.9:c.*161A>T MANE Select	ENSP00000373477.4:n.*161A>T
ENST00000388825.8:c.*161A>T	ENSP00000373477.4:n.*161A>T
ENST00000521632.1:c.651A>T
ENST00000614343.4:c.*623A>T	ENSP00000483660.1:n.*623A>T
ENST00000622181.4:c.*161A>T	ENSP00000484258.1:n.*161A>T
NM_002084.3:c.*161A>T	NP_002075.2:n.*161A>T
NM_001329790.1:c.*161A>T	NP_001316719.1:n.*161A>T
NM_002084.4:c.*161A>T	NP_002075.2:n.*161A>T
NM_002084.5:c.*161A>T MANE Select	NP_002075.2:n.*161A>T
NM_001329790.2:c.*161A>T	NP_001316719.1:n.*161A>T