Canonical Allele Identifier: CA2317520648

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106413A= , CM000681.2:g.1106413A=	GRCh38
NC_000019.9:g.1106412A= , CM000681.1:g.1106412A=	GRCh37
NC_000019.8:g.1057412A=	NCBI36
NG_050621.1:g.7488A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.626A=	ENSP00000473614.3:p.Lys209=
ENST00000593032.6:c.495A=	ENSP00000465828.4:p.Gln165=
ENST00000706713.1:c.509A=	ENSP00000516510.1:p.Lys170=
ENST00000706714.1:c.495A=	ENSP00000516511.1:p.Gln165=
ENST00000706715.1:c.131A=	ENSP00000516512.1:p.Lys44=
ENST00000354171.13:c.515A= MANE Select	ENSP00000346103.7:p.Lys172=
ENST00000589115.6:c.490A=	ENSP00000466872.3:p.Arg164=
ENST00000354171.12:c.515A=	ENSP00000346103.7:p.Lys172=
ENST00000585480.1:c.248A=	ENSP00000467900.1:p.Lys83=
ENST00000587648.5:c.395A=	ENSP00000468349.1:p.Lys132=
ENST00000588919.5:c.456A=	ENSP00000464989.3:p.Gln152=
ENST00000589115.5:c.490A=	ENSP00000466872.2:p.Arg164=
ENST00000592940.2:n.886A=
ENST00000593032.5:c.495A=	ENSP00000465828.3:p.Gln165=
ENST00000611653.4:c.434A=	ENSP00000483655.1:p.Lys145=
ENST00000616066.4:c.512A=	ENSP00000485000.1:p.Lys171=
ENST00000622390.4:c.623A=	ENSP00000477503.1:p.Lys208=
NM_001039847.2:c.537A=	NP_001034936.1:p.Gln179=
NM_001039848.2:c.626A=	NP_001034937.1:p.Lys209=
NM_002085.4:c.515A=	NP_002076.2:p.Lys172=
NM_001039848.3:c.626A=	NP_001034937.1:p.Lys209=
NM_001039847.3:c.537A=	NP_001034936.1:p.Gln179=
NM_001039848.4:c.626A=	NP_001034937.1:p.Lys209=
NM_001367832.1:c.434A=	NP_001354761.1:p.Lys145=
NM_002085.5:c.515A= MANE Select	NP_002076.2:p.Lys172=