Canonical Allele Identifier: CA402939691

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106405A>T (hg19) ; chr19:g.1106406A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106406A>T , CM000681.2:g.1106406A>T	GRCh38
NC_000019.9:g.1106405A>T , CM000681.1:g.1106405A>T	GRCh37
NC_000019.8:g.1057405A>T	NCBI36
NG_050621.1:g.7481A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.619A>T	ENSP00000473614.3:p.Ile207Phe
ENST00000593032.6:c.488A>T	ENSP00000465828.4:p.His163Leu
ENST00000706713.1:c.502A>T	ENSP00000516510.1:p.Ile168Phe
ENST00000706714.1:c.488A>T	ENSP00000516511.1:p.His163Leu
ENST00000706715.1:c.124A>T	ENSP00000516512.1:p.Ile42Phe
ENST00000354171.13:c.508A>T MANE Select	ENSP00000346103.7:p.Ile170Phe
ENST00000589115.6:c.483A>T	ENSP00000466872.3:p.Ser161=
ENST00000354171.12:c.508A>T	ENSP00000346103.7:p.Ile170Phe
ENST00000585480.1:c.241A>T	ENSP00000467900.1:p.Ile81Phe
ENST00000587648.5:c.388A>T	ENSP00000468349.1:p.Ile130Phe
ENST00000588919.5:c.449A>T	ENSP00000464989.3:p.His150Leu
ENST00000589115.5:c.483A>T	ENSP00000466872.2:p.Ser161=
ENST00000592940.2:n.879A>T
ENST00000593032.5:c.488A>T	ENSP00000465828.3:p.His163Leu
ENST00000611653.4:c.427A>T	ENSP00000483655.1:p.Ile143Phe
ENST00000616066.4:c.505A>T	ENSP00000485000.1:p.Ile169Phe
ENST00000622390.4:c.616A>T	ENSP00000477503.1:p.Ile206Phe
NM_001039847.2:c.530A>T	NP_001034936.1:p.His177Leu
NM_001039848.2:c.619A>T	NP_001034937.1:p.Ile207Phe
NM_002085.4:c.508A>T	NP_002076.2:p.Ile170Phe
NM_001039848.3:c.619A>T	NP_001034937.1:p.Ile207Phe
NM_001039847.3:c.530A>T	NP_001034936.1:p.His177Leu
NM_001039848.4:c.619A>T	NP_001034937.1:p.Ile207Phe
NM_001367832.1:c.427A>T	NP_001354761.1:p.Ile143Phe
NM_002085.5:c.508A>T MANE Select	NP_002076.2:p.Ile170Phe