Canonical Allele Identifier: CA402939263

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106263A>T (hg19) ; chr19:g.1106264A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106264A>T , CM000681.2:g.1106264A>T	GRCh38
NC_000019.9:g.1106263A>T , CM000681.1:g.1106263A>T	GRCh37
NC_000019.8:g.1057263A>T	NCBI36
NG_050621.1:g.7339A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.610A>T	ENSP00000473614.3:p.Lys204Ter
ENST00000593032.6:c.479A>T	ENSP00000465828.4:p.Gln160Leu
ENST00000706713.1:c.493A>T	ENSP00000516510.1:p.Lys165Ter
ENST00000706714.1:c.479A>T	ENSP00000516511.1:p.Gln160Leu
ENST00000706715.1:c.115A>T	ENSP00000516512.1:p.Lys39Ter
ENST00000354171.13:c.499A>T MANE Select	ENSP00000346103.7:p.Lys167Ter
ENST00000589115.6:c.477-136A>T	ENSP00000466872.3:n.477-136A>T
ENST00000354171.12:c.499A>T	ENSP00000346103.7:p.Lys167Ter
ENST00000585480.1:c.232A>T	ENSP00000467900.1:p.Lys78Ter
ENST00000587648.5:c.379A>T	ENSP00000468349.1:p.Lys127Ter
ENST00000588919.5:c.418A>T	ENSP00000464989.3:p.Lys140Ter
ENST00000589115.5:c.477-136A>T	ENSP00000466872.2:n.477-136A>T
ENST00000592940.2:n.870A>T
ENST00000593032.5:c.479A>T	ENSP00000465828.3:p.Gln160Leu
ENST00000611653.4:c.418A>T	ENSP00000483655.1:p.Lys140Ter
ENST00000616066.4:c.496A>T	ENSP00000485000.1:p.Lys166Ter
ENST00000622390.4:c.607A>T	ENSP00000477503.1:p.Lys203Ter
NM_001039847.2:c.499A>T	NP_001034936.1:p.Lys167Ter
NM_001039848.2:c.610A>T	NP_001034937.1:p.Lys204Ter
NM_002085.4:c.499A>T	NP_002076.2:p.Lys167Ter
NM_001039848.3:c.610A>T	NP_001034937.1:p.Lys204Ter
NM_001039847.3:c.499A>T	NP_001034936.1:p.Lys167Ter
NM_001039848.4:c.610A>T	NP_001034937.1:p.Lys204Ter
NM_001367832.1:c.418A>T	NP_001354761.1:p.Lys140Ter
NM_002085.5:c.499A>T MANE Select	NP_002076.2:p.Lys167Ter