Canonical Allele Identifier: CA1591209960

Gene: GPX3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028282T= , CM000667.2:g.151028282T=	GRCh38
NC_000005.9:g.150407843T= , CM000667.1:g.150407843T=	GRCh37
NC_000005.8:g.150388036T=	NCBI36
NG_030590.1:g.64379A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000388825.9:c.*152T= MANE Select	ENSP00000373477.4:n.*152T=
ENST00000388825.8:c.*152T=	ENSP00000373477.4:n.*152T=
ENST00000521632.1:c.642T=
ENST00000614343.4:c.*614T=	ENSP00000483660.1:n.*614T=
ENST00000622181.4:c.*152T=	ENSP00000484258.1:n.*152T=
NM_002084.3:c.*152T=	NP_002075.2:n.*152T=
NM_001329790.1:c.*152T=	NP_001316719.1:n.*152T=
NM_002084.4:c.*152T=	NP_002075.2:n.*152T=
NM_002084.5:c.*152T= MANE Select	NP_002075.2:n.*152T=
NM_001329790.2:c.*152T=	NP_001316719.1:n.*152T=