Canonical Allele Identifier: CA1363446851

Gene: GPX1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_000581.4:c.599C= MANE Select	NP_000572.2:p.Pro200=
ENST00000419783.3:c.599C= MANE Select	ENSP00000407375.1:p.Pro200=
NM_000581.2:c.599C=	NP_000572.2:p.Pro200=
NM_000581.3:c.599C=	NP_000572.2:p.Pro200=
NM_001329455.1:c.461C=	NP_001316384.1:p.Pro154=
NM_001329455.2:c.461C=	NP_001316384.1:p.Pro154=
NM_001329502.1:c.*425C=	NP_001316431.1:n.*425C=
NM_001329502.2:c.*425C=	NP_001316431.1:n.*425C=
NM_001329503.1:c.*105C=	NP_001316432.1:n.*105C=
NM_001329503.2:c.*105C=	NP_001316432.1:n.*105C=
NM_201397.1:c.*581C=	NP_958799.1:n.*581C=
NM_201397.2:c.*581C=	NP_958799.1:n.*581C=
NM_201397.3:c.*581C=	NP_958799.1:n.*581C=
ENST00000419349.1:c.*581C=	ENSP00000391316.1:n.*581C=
ENST00000419349.2:c.*581C=	ENSP00000391316.1:n.*581C=
ENST00000419349.3:c.*581C=	ENSP00000391316.1:n.*581C=
ENST00000419783.1:c.599C=	ENSP00000407375.1:p.Pro200=
ENST00000496791.3:c.*425C=	ENSP00000493593.2:n.*425C=
ENST00000620890.1:c.596C=	ENSP00000478837.1:p.Pro199=
ENST00000643797.1:c.461C=	ENSP00000495108.1:p.Pro154=
ENST00000643797.2:c.461C=	ENSP00000495108.1:p.Pro154=
ENST00000646881.3:c.*105C=	ENSP00000495001.2:n.*105C=
ENST00000703795.1:c.596C=	ENSP00000515480.1:p.Pro199=
ENST00000703796.1:c.560C=	ENSP00000515481.1:p.Pro187=
ENST00000703797.1:c.*492C=	ENSP00000515482.1:n.*492C=
ENST00000704356.1:c.356C=	ENSP00000515867.1:p.Pro119=
ENST00000704374.1:c.434C=	ENSP00000515879.1:p.Pro145=
ENST00000704375.1:c.*373C=	ENSP00000515880.1:n.*373C=
ENST00000704376.1:c.*39C=	ENSP00000515881.1:n.*39C=
ENST00000704377.1:c.*39C=	ENSP00000515882.1:n.*39C=
ENST00000704378.1:c.*39C=	ENSP00000515883.1:n.*39C=
ENST00000704379.1:n.472C=
ENST00000704380.1:n.432C=
ENST00000704381.1:c.*319C=	ENSP00000515884.1:n.*319C=