Canonical Allele Identifier: CA402940092

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106443C>A (hg19) ; chr19:g.1106444C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106444C>A , CM000681.2:g.1106444C>A	GRCh38
NC_000019.9:g.1106443C>A , CM000681.1:g.1106443C>A	GRCh37
NC_000019.8:g.1057443C>A	NCBI36
NG_050621.1:g.7519C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.657C>A	ENSP00000473614.3:p.Pro219=
ENST00000593032.6:c.526C>A	ENSP00000465828.4:p.His176Asn
ENST00000706713.1:c.540C>A	ENSP00000516510.1:p.Pro180=
ENST00000706714.1:c.526C>A	ENSP00000516511.1:p.His176Asn
ENST00000706715.1:c.162C>A	ENSP00000516512.1:p.Pro54=
ENST00000354171.13:c.546C>A MANE Select	ENSP00000346103.7:p.Pro182=
ENST00000589115.6:c.521C>A	ENSP00000466872.3:p.Pro174Gln
ENST00000354171.12:c.546C>A	ENSP00000346103.7:p.Pro182=
ENST00000585480.1:c.279C>A	ENSP00000467900.1:p.Pro93=
ENST00000587648.5:c.426C>A	ENSP00000468349.1:p.Pro142=
ENST00000588919.5:c.487C>A	ENSP00000464989.3:p.His163Asn
ENST00000589115.5:c.521C>A	ENSP00000466872.2:p.Pro174Gln
ENST00000592940.2:n.917C>A
ENST00000611653.4:c.465C>A	ENSP00000483655.1:p.Pro155=
ENST00000616066.4:c.543C>A	ENSP00000485000.1:p.Pro181=
ENST00000622390.4:c.654C>A	ENSP00000477503.1:p.Pro218=
NM_001039847.2:c.568C>A	NP_001034936.1:p.His190Asn
NM_001039848.2:c.657C>A	NP_001034937.1:p.Pro219=
NM_002085.4:c.546C>A	NP_002076.2:p.Pro182=
NM_001039848.3:c.657C>A	NP_001034937.1:p.Pro219=
NM_001039847.3:c.568C>A	NP_001034936.1:p.His190Asn
NM_001039848.4:c.657C>A	NP_001034937.1:p.Pro219=
NM_001367832.1:c.465C>A	NP_001354761.1:p.Pro155=
NM_002085.5:c.546C>A MANE Select	NP_002076.2:p.Pro182=