Canonical Allele Identifier: CA352781901
Gene: GPX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49357401G>T , CM000665.2:g.49357401G>T GRCh38
NC_000003.11:g.49394834G>T , CM000665.1:g.49394834G>T GRCh37
NC_000003.10:g.49369838G>T NCBI36
NG_012264.1:g.5958C>A
NG_051308.1:g.59697C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000581.4:c.599C>A MANE Select NP_000572.2:p.Pro200His
ENST00000419783.3:c.599C>A MANE Select ENSP00000407375.1:p.Pro200His
NM_000581.2:c.599C>A NP_000572.2:p.Pro200His
NM_000581.3:c.599C>A NP_000572.2:p.Pro200His
NM_001329455.1:c.461C>A NP_001316384.1:p.Pro154His
NM_001329455.2:c.461C>A NP_001316384.1:p.Pro154His
NM_001329502.1:c.*425C>A NP_001316431.1:n.*425C>A
NM_001329502.2:c.*425C>A NP_001316431.1:n.*425C>A
NM_001329503.1:c.*105C>A NP_001316432.1:n.*105C>A
NM_001329503.2:c.*105C>A NP_001316432.1:n.*105C>A
NM_201397.1:c.*581C>A NP_958799.1:n.*581C>A
NM_201397.2:c.*581C>A NP_958799.1:n.*581C>A
NM_201397.3:c.*581C>A NP_958799.1:n.*581C>A
ENST00000419349.1:c.*581C>A ENSP00000391316.1:n.*581C>A
ENST00000419349.2:c.*581C>A ENSP00000391316.1:n.*581C>A
ENST00000419349.3:c.*581C>A ENSP00000391316.1:n.*581C>A
ENST00000419783.1:c.599C>A ENSP00000407375.1:p.Pro200His
ENST00000496791.3:c.*425C>A ENSP00000493593.2:n.*425C>A
ENST00000620890.1:c.596C>A ENSP00000478837.1:p.Pro199His
ENST00000643797.1:c.461C>A ENSP00000495108.1:p.Pro154His
ENST00000643797.2:c.461C>A ENSP00000495108.1:p.Pro154His
ENST00000646881.3:c.*105C>A ENSP00000495001.2:n.*105C>A
ENST00000703795.1:c.596C>A ENSP00000515480.1:p.Pro199His
ENST00000703796.1:c.560C>A ENSP00000515481.1:p.Pro187His
ENST00000703797.1:c.*492C>A ENSP00000515482.1:n.*492C>A
ENST00000704356.1:c.356C>A ENSP00000515867.1:p.Pro119His
ENST00000704374.1:c.434C>A ENSP00000515879.1:p.Pro145His
ENST00000704375.1:c.*373C>A ENSP00000515880.1:n.*373C>A
ENST00000704376.1:c.*39C>A ENSP00000515881.1:n.*39C>A
ENST00000704377.1:c.*39C>A ENSP00000515882.1:n.*39C>A
ENST00000704378.1:c.*39C>A ENSP00000515883.1:n.*39C>A
ENST00000704379.1:n.472C>A
ENST00000704380.1:n.432C>A
ENST00000704381.1:c.*319C>A ENSP00000515884.1:n.*319C>A