Canonical Allele Identifier: CA1363447496

Gene: GPX1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49358324G= , CM000665.2:g.49358324G=	GRCh38
NC_000003.11:g.49395757G= , CM000665.1:g.49395757G=	GRCh37
NC_000003.10:g.49370761G=	NCBI36
NG_012264.1:g.5035C=
NG_051308.1:g.58774C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496791.3:c.-46C=	ENSP00000493593.2:n.-46C=
ENST00000643797.2:c.-46C=	ENSP00000495108.1:n.-46C=
ENST00000646881.3:c.-46C=	ENSP00000495001.2:n.-46C=
ENST00000703795.1:c.-46C=	ENSP00000515480.1:n.-46C=
ENST00000703797.1:c.-46C=	ENSP00000515482.1:n.-46C=
ENST00000704356.1:c.-46C=	ENSP00000515867.1:n.-46C=
ENST00000704375.1:c.-46C=	ENSP00000515880.1:n.-46C=
ENST00000704377.1:c.-46C=	ENSP00000515882.1:n.-46C=
ENST00000704378.1:c.-46C=	ENSP00000515883.1:n.-46C=
ENST00000704379.1:n.125+492C=
ENST00000704380.1:n.86-577C=
ENST00000704381.1:c.465-577C=	ENSP00000515884.1:n.465-577C=
ENST00000419783.3:c.-46C= MANE Select	ENSP00000407375.1:n.-46C=
ENST00000496791.2:c.-46C=	ENSP00000493593.2:n.-46C=
ENST00000643797.1:c.-46C=	ENSP00000495108.1:n.-46C=
ENST00000646881.2:c.-46C=	ENSP00000495001.2:n.-46C=
ENST00000419783.1:c.-46C=	ENSP00000407375.1:n.-46C=
ENST00000496791.1:n.2C=
ENST00000620890.1:c.-46C=	ENSP00000478837.1:n.-46C=
NM_000581.2:c.-46C=	NP_000572.2:n.-46C=
NM_201397.1:c.-46C=	NP_958799.1:n.-46C=
NM_000581.3:c.-46C=	NP_000572.2:n.-46C=
NM_001329455.1:c.-46C=	NP_001316384.1:n.-46C=
NM_001329502.1:c.-46C=	NP_001316431.1:n.-46C=
NM_001329503.1:c.-46C=	NP_001316432.1:n.-46C=
NM_201397.2:c.-46C=	NP_958799.1:n.-46C=
NM_000581.4:c.-46C= MANE Select	NP_000572.2:n.-46C=
NM_001329502.2:c.-46C=	NP_001316431.1:n.-46C=
NM_001329503.2:c.-46C=	NP_001316432.1:n.-46C=
NM_201397.3:c.-46C=	NP_958799.1:n.-46C=
NM_001329455.2:c.-46C=	NP_001316384.1:n.-46C=