Canonical Allele Identifier: CA504890902

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105701C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105702C>T , CM000681.2:g.1105702C>T	GRCh38
NC_000019.9:g.1105701C>T , CM000681.1:g.1105701C>T	GRCh37
NC_000019.8:g.1056701C>T	NCBI36
NG_050621.1:g.6777C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.480C>T	ENSP00000473614.3:p.Tyr160=
ENST00000593032.6:c.288C>T	ENSP00000465828.4:p.Tyr96=
ENST00000706713.1:c.363C>T	ENSP00000516510.1:p.Tyr121=
ENST00000706714.1:c.288C>T	ENSP00000516511.1:p.Tyr96=
ENST00000706715.1:c.-16C>T	ENSP00000516512.1:n.-16C>T
ENST00000354171.13:c.369C>T MANE Select	ENSP00000346103.7:p.Tyr123=
ENST00000589115.6:c.369C>T	ENSP00000466872.3:p.Tyr123=
ENST00000354171.12:c.369C>T	ENSP00000346103.7:p.Tyr123=
ENST00000585362.6:c.480C>T	ENSP00000473614.2:p.Tyr160=
ENST00000585480.1:c.102C>T	ENSP00000467900.1:p.Tyr34=
ENST00000587648.5:c.249C>T	ENSP00000468349.1:p.Tyr83=
ENST00000588919.5:c.288C>T	ENSP00000464989.3:p.Tyr96=
ENST00000589115.5:c.369C>T	ENSP00000466872.2:p.Tyr123=
ENST00000592940.2:n.308C>T
ENST00000593032.5:c.288C>T	ENSP00000465828.3:p.Tyr96=
ENST00000611653.4:c.288C>T	ENSP00000483655.1:p.Tyr96=
ENST00000616066.4:c.366C>T	ENSP00000485000.1:p.Tyr122=
ENST00000622390.4:c.477C>T	ENSP00000477503.1:p.Tyr159=
NM_001039847.2:c.369C>T	NP_001034936.1:p.Tyr123=
NM_001039848.2:c.480C>T	NP_001034937.1:p.Tyr160=
NM_002085.4:c.369C>T	NP_002076.2:p.Tyr123=
NM_001039848.3:c.480C>T	NP_001034937.1:p.Tyr160=
NM_001039847.3:c.369C>T	NP_001034936.1:p.Tyr123=
NM_001039848.4:c.480C>T	NP_001034937.1:p.Tyr160=
NM_001367832.1:c.288C>T	NP_001354761.1:p.Tyr96=
NM_002085.5:c.369C>T MANE Select	NP_002076.2:p.Tyr123=