Canonical Allele Identifier: CA2317520107

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105724A= , CM000681.2:g.1105724A=	GRCh38
NC_000019.9:g.1105723A= , CM000681.1:g.1105723A=	GRCh37
NC_000019.8:g.1056723A=	NCBI36
NG_050621.1:g.6799A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.502A=	ENSP00000473614.3:p.Ser168=
ENST00000593032.6:c.310A=	ENSP00000465828.4:p.Ser104=
ENST00000706713.1:c.385A=	ENSP00000516510.1:p.Ser129=
ENST00000706714.1:c.310A=	ENSP00000516511.1:p.Ser104=
ENST00000706715.1:c.7A=	ENSP00000516512.1:p.Ser3=
ENST00000354171.13:c.391A= MANE Select	ENSP00000346103.7:p.Ser131=
ENST00000589115.6:c.391A=	ENSP00000466872.3:p.Ser131=
ENST00000354171.12:c.391A=	ENSP00000346103.7:p.Ser131=
ENST00000585362.6:c.502A=	ENSP00000473614.2:p.Ser168=
ENST00000585480.1:c.124A=	ENSP00000467900.1:p.Ser42=
ENST00000587648.5:c.271A=	ENSP00000468349.1:p.Ser91=
ENST00000588919.5:c.310A=	ENSP00000464989.3:p.Ser104=
ENST00000589115.5:c.391A=	ENSP00000466872.2:p.Ser131=
ENST00000592940.2:n.330A=
ENST00000593032.5:c.310A=	ENSP00000465828.3:p.Ser104=
ENST00000611653.4:c.310A=	ENSP00000483655.1:p.Ser104=
ENST00000616066.4:c.388A=	ENSP00000485000.1:p.Ser130=
ENST00000622390.4:c.499A=	ENSP00000477503.1:p.Ser167=
NM_001039847.2:c.391A=	NP_001034936.1:p.Ser131=
NM_001039848.2:c.502A=	NP_001034937.1:p.Ser168=
NM_002085.4:c.391A=	NP_002076.2:p.Ser131=
NM_001039848.3:c.502A=	NP_001034937.1:p.Ser168=
NM_001039847.3:c.391A=	NP_001034936.1:p.Ser131=
NM_001039848.4:c.502A=	NP_001034937.1:p.Ser168=
NM_001367832.1:c.310A=	NP_001354761.1:p.Ser104=
NM_002085.5:c.391A= MANE Select	NP_002076.2:p.Ser131=