Canonical Allele Identifier: CA2676036224
Gene: GPX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151028394T>A , CM000667.2:g.151028394T>A GRCh38
NC_000005.9:g.150407955T>A , CM000667.1:g.150407955T>A GRCh37
NC_000005.8:g.150388148T>A NCBI36
NG_030590.1:g.64267A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000388825.9:c.*264T>A MANE Select ENSP00000373477.4:n.*264T>A
ENST00000388825.8:c.*264T>A ENSP00000373477.4:n.*264T>A
ENST00000521632.1:c.754T>A
ENST00000614343.4:c.*726T>A ENSP00000483660.1:n.*726T>A
ENST00000622181.4:c.*264T>A ENSP00000484258.1:n.*264T>A
NM_002084.3:c.*264T>A NP_002075.2:n.*264T>A
NM_001329790.1:c.*264T>A NP_001316719.1:n.*264T>A
NM_002084.4:c.*264T>A NP_002075.2:n.*264T>A
NM_002084.5:c.*264T>A MANE Select NP_002075.2:n.*264T>A
NM_001329790.2:c.*264T>A NP_001316719.1:n.*264T>A