Canonical Allele Identifier: CA2317520120

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105747C= , CM000681.2:g.1105747C=	GRCh38
NC_000019.9:g.1105746C= , CM000681.1:g.1105746C=	GRCh37
NC_000019.8:g.1056746C=	NCBI36
NG_050621.1:g.6822C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.525C=	ENSP00000473614.3:p.Asp175=
ENST00000593032.6:c.333C=	ENSP00000465828.4:p.Asp111=
ENST00000706713.1:c.408C=	ENSP00000516510.1:p.Asp136=
ENST00000706714.1:c.333C=	ENSP00000516511.1:p.Asp111=
ENST00000706715.1:c.30C=	ENSP00000516512.1:p.Asp10=
ENST00000354171.13:c.414C= MANE Select	ENSP00000346103.7:p.Asp138=
ENST00000589115.6:c.414C=	ENSP00000466872.3:p.Asp138=
ENST00000354171.12:c.414C=	ENSP00000346103.7:p.Asp138=
ENST00000585362.6:c.525C=	ENSP00000473614.2:p.Asp175=
ENST00000585480.1:c.147C=	ENSP00000467900.1:p.Asp49=
ENST00000587648.5:c.294C=	ENSP00000468349.1:p.Asp98=
ENST00000588919.5:c.333C=	ENSP00000464989.3:p.Asp111=
ENST00000589115.5:c.414C=	ENSP00000466872.2:p.Asp138=
ENST00000592940.2:n.353C=
ENST00000593032.5:c.333C=	ENSP00000465828.3:p.Asp111=
ENST00000611653.4:c.333C=	ENSP00000483655.1:p.Asp111=
ENST00000616066.4:c.411C=	ENSP00000485000.1:p.Asp137=
ENST00000622390.4:c.522C=	ENSP00000477503.1:p.Asp174=
NM_001039847.2:c.414C=	NP_001034936.1:p.Asp138=
NM_001039848.2:c.525C=	NP_001034937.1:p.Asp175=
NM_002085.4:c.414C=	NP_002076.2:p.Asp138=
NM_001039848.3:c.525C=	NP_001034937.1:p.Asp175=
NM_001039847.3:c.414C=	NP_001034936.1:p.Asp138=
NM_001039848.4:c.525C=	NP_001034937.1:p.Asp175=
NM_001367832.1:c.333C=	NP_001354761.1:p.Asp111=
NM_002085.5:c.414C= MANE Select	NP_002076.2:p.Asp138=