Canonical Allele Identifier: CA402939648

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106402C>T (hg19) ; chr19:g.1106403C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106403C>T , CM000681.2:g.1106403C>T	GRCh38
NC_000019.9:g.1106402C>T , CM000681.1:g.1106402C>T	GRCh37
NC_000019.8:g.1057402C>T	NCBI36
NG_050621.1:g.7478C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.616C>T	ENSP00000473614.3:p.Leu206Phe
ENST00000593032.6:c.485C>T	ENSP00000465828.4:p.Pro162Leu
ENST00000706713.1:c.499C>T	ENSP00000516510.1:p.Leu167Phe
ENST00000706714.1:c.485C>T	ENSP00000516511.1:p.Pro162Leu
ENST00000706715.1:c.121C>T	ENSP00000516512.1:p.Leu41Phe
ENST00000354171.13:c.505C>T MANE Select	ENSP00000346103.7:p.Leu169Phe
ENST00000589115.6:c.480C>T	ENSP00000466872.3:p.Ser160=
ENST00000354171.12:c.505C>T	ENSP00000346103.7:p.Leu169Phe
ENST00000585480.1:c.238C>T	ENSP00000467900.1:p.Leu80Phe
ENST00000587648.5:c.385C>T	ENSP00000468349.1:p.Leu129Phe
ENST00000588919.5:c.446C>T	ENSP00000464989.3:p.Pro149Leu
ENST00000589115.5:c.480C>T	ENSP00000466872.2:p.Ser160=
ENST00000592940.2:n.876C>T
ENST00000593032.5:c.485C>T	ENSP00000465828.3:p.Pro162Leu
ENST00000611653.4:c.424C>T	ENSP00000483655.1:p.Leu142Phe
ENST00000616066.4:c.502C>T	ENSP00000485000.1:p.Leu168Phe
ENST00000622390.4:c.613C>T	ENSP00000477503.1:p.Leu205Phe
NM_001039847.2:c.527C>T	NP_001034936.1:p.Pro176Leu
NM_001039848.2:c.616C>T	NP_001034937.1:p.Leu206Phe
NM_002085.4:c.505C>T	NP_002076.2:p.Leu169Phe
NM_001039848.3:c.616C>T	NP_001034937.1:p.Leu206Phe
NM_001039847.3:c.527C>T	NP_001034936.1:p.Pro176Leu
NM_001039848.4:c.616C>T	NP_001034937.1:p.Leu206Phe
NM_001367832.1:c.424C>T	NP_001354761.1:p.Leu142Phe
NM_002085.5:c.505C>T MANE Select	NP_002076.2:p.Leu169Phe