Canonical Allele Identifier: CA352783332

Gene: GPX1

Linked Data

• MyVariant Identifiers: chr3:g.49395561T>C (hg19) ; chr3:g.49358128T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49358128T>C , CM000665.2:g.49358128T>C	GRCh38
NC_000003.11:g.49395561T>C , CM000665.1:g.49395561T>C	GRCh37
NC_000003.10:g.49370565T>C	NCBI36
NG_012264.1:g.5231A>G
NG_051308.1:g.58970A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419349.3:c.151A>G	ENSP00000391316.1:p.Thr51Ala
ENST00000496791.3:c.151A>G	ENSP00000493593.2:p.Thr51Ala
ENST00000643797.2:c.114+37A>G	ENSP00000495108.1:n.114+37A>G
ENST00000646881.3:c.151A>G	ENSP00000495001.2:p.Thr51Ala
ENST00000703795.1:c.151A>G	ENSP00000515480.1:p.Thr51Ala
ENST00000703796.1:c.151A>G	ENSP00000515481.1:p.Thr51Ala
ENST00000703797.1:c.151A>G	ENSP00000515482.1:p.Thr51Ala
ENST00000704356.1:c.151A>G	ENSP00000515867.1:p.Thr51Ala
ENST00000704374.1:c.87+64A>G	ENSP00000515879.1:n.87+64A>G
ENST00000704375.1:c.151A>G	ENSP00000515880.1:p.Thr51Ala
ENST00000704376.1:c.148+3A>G	ENSP00000515881.1:n.148+3A>G
ENST00000704377.1:c.114+37A>G	ENSP00000515882.1:n.114+37A>G
ENST00000704378.1:c.151A>G	ENSP00000515883.1:p.Thr51Ala
ENST00000704379.1:n.126-381A>G
ENST00000704380.1:n.86-381A>G
ENST00000704381.1:c.465-381A>G	ENSP00000515884.1:n.465-381A>G
ENST00000419349.2:c.151A>G	ENSP00000391316.1:p.Thr51Ala
ENST00000419783.3:c.151A>G MANE Select	ENSP00000407375.1:p.Thr51Ala
ENST00000496791.2:c.151A>G	ENSP00000493593.2:p.Thr51Ala
ENST00000643797.1:c.114+37A>G	ENSP00000495108.1:n.114+37A>G
ENST00000646881.2:c.151A>G	ENSP00000495001.2:p.Thr51Ala
ENST00000419349.1:c.151A>G	ENSP00000391316.1:p.Thr51Ala
ENST00000419783.1:c.151A>G	ENSP00000407375.1:p.Thr51Ala
ENST00000496791.1:n.198A>G
ENST00000620890.1:c.148A>G	ENSP00000478837.1:p.Thr50Ala
NM_000581.2:c.151A>G	NP_000572.2:p.Thr51Ala
NM_201397.1:c.151A>G	NP_958799.1:p.Thr51Ala
NM_000581.3:c.151A>G	NP_000572.2:p.Thr51Ala
NM_001329455.1:c.114+37A>G	NP_001316384.1:n.114+37A>G
NM_001329502.1:c.151A>G	NP_001316431.1:p.Thr51Ala
NM_001329503.1:c.151A>G	NP_001316432.1:p.Thr51Ala
NM_201397.2:c.151A>G	NP_958799.1:p.Thr51Ala
NM_000581.4:c.151A>G MANE Select	NP_000572.2:p.Thr51Ala
NM_001329502.2:c.151A>G	NP_001316431.1:p.Thr51Ala
NM_001329503.2:c.151A>G	NP_001316432.1:p.Thr51Ala
NM_201397.3:c.151A>G	NP_958799.1:p.Thr51Ala
NM_001329455.2:c.114+37A>G	NP_001316384.1:n.114+37A>G