Canonical Allele Identifier: CA9037260

Gene: GPX4

Linked Data

• dbSNP Id: rs769967246
• ExAC: 19:1105455 C / T
• gnomAD v2: 19-1105455-C-T
• gnomAD v3: 19-1105456-C-T
• gnomAD v4: 19-1105456-C-T
• MyVariant Identifiers: chr19:g.1105455C>T (hg19) ; chr19:g.1105456C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105456C>T , CM000681.2:g.1105456C>T	GRCh38
NC_000019.9:g.1105455C>T , CM000681.1:g.1105455C>T	GRCh37
NC_000019.8:g.1056455C>T	NCBI36
NG_050621.1:g.6531C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.381C>T	ENSP00000473614.3:p.Tyr127=
ENST00000593032.6:c.189C>T	ENSP00000465828.4:p.Tyr63=
ENST00000706713.1:c.264C>T	ENSP00000516510.1:p.Tyr88=
ENST00000706714.1:c.189C>T	ENSP00000516511.1:p.Tyr63=
ENST00000706715.1:c.-115C>T	ENSP00000516512.1:n.-115C>T
ENST00000354171.13:c.270C>T MANE Select	ENSP00000346103.7:p.Tyr90=
ENST00000589115.6:c.270C>T	ENSP00000466872.3:p.Tyr90=
ENST00000354171.12:c.270C>T	ENSP00000346103.7:p.Tyr90=
ENST00000585362.6:c.381C>T	ENSP00000473614.2:p.Tyr127=
ENST00000585480.1:c.3C>T	ENSP00000467900.1:p.Tyr1=
ENST00000587648.5:c.150C>T	ENSP00000468349.1:p.Tyr50=
ENST00000587932.2:n.204C>T
ENST00000588919.5:c.189C>T	ENSP00000464989.3:p.Tyr63=
ENST00000589115.5:c.270C>T	ENSP00000466872.2:p.Tyr90=
ENST00000592940.2:n.216C>T
ENST00000593032.5:c.189C>T	ENSP00000465828.3:p.Tyr63=
ENST00000611653.4:c.189C>T	ENSP00000483655.1:p.Tyr63=
ENST00000614791.1:c.375C>T	ENSP00000484697.1:p.Tyr125=
ENST00000616066.4:c.267C>T	ENSP00000485000.1:p.Tyr89=
ENST00000622390.4:c.378C>T	ENSP00000477503.1:p.Tyr126=
NM_001039847.2:c.270C>T	NP_001034936.1:p.Tyr90=
NM_001039848.2:c.381C>T	NP_001034937.1:p.Tyr127=
NM_002085.4:c.270C>T	NP_002076.2:p.Tyr90=
NM_001039848.3:c.381C>T	NP_001034937.1:p.Tyr127=
NM_001039847.3:c.270C>T	NP_001034936.1:p.Tyr90=
NM_001039848.4:c.381C>T	NP_001034937.1:p.Tyr127=
NM_001367832.1:c.189C>T	NP_001354761.1:p.Tyr63=
NM_002085.5:c.270C>T MANE Select	NP_002076.2:p.Tyr90=