Canonical Allele Identifier: CA402937549

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105733G>A (hg19) ; chr19:g.1105734G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105734G>A , CM000681.2:g.1105734G>A	GRCh38
NC_000019.9:g.1105733G>A , CM000681.1:g.1105733G>A	GRCh37
NC_000019.8:g.1056733G>A	NCBI36
NG_050621.1:g.6809G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.512G>A	ENSP00000473614.3:p.Cys171Tyr
ENST00000593032.6:c.320G>A	ENSP00000465828.4:p.Cys107Tyr
ENST00000706713.1:c.395G>A	ENSP00000516510.1:p.Cys132Tyr
ENST00000706714.1:c.320G>A	ENSP00000516511.1:p.Cys107Tyr
ENST00000706715.1:c.17G>A	ENSP00000516512.1:p.Cys6Tyr
ENST00000354171.13:c.401G>A MANE Select	ENSP00000346103.7:p.Cys134Tyr
ENST00000589115.6:c.401G>A	ENSP00000466872.3:p.Cys134Tyr
ENST00000354171.12:c.401G>A	ENSP00000346103.7:p.Cys134Tyr
ENST00000585362.6:c.512G>A	ENSP00000473614.2:p.Cys171Tyr
ENST00000585480.1:c.134G>A	ENSP00000467900.1:p.Cys45Tyr
ENST00000587648.5:c.281G>A	ENSP00000468349.1:p.Cys94Tyr
ENST00000588919.5:c.320G>A	ENSP00000464989.3:p.Cys107Tyr
ENST00000589115.5:c.401G>A	ENSP00000466872.2:p.Cys134Tyr
ENST00000592940.2:n.340G>A
ENST00000593032.5:c.320G>A	ENSP00000465828.3:p.Cys107Tyr
ENST00000611653.4:c.320G>A	ENSP00000483655.1:p.Cys107Tyr
ENST00000616066.4:c.398G>A	ENSP00000485000.1:p.Cys133Tyr
ENST00000622390.4:c.509G>A	ENSP00000477503.1:p.Cys170Tyr
NM_001039847.2:c.401G>A	NP_001034936.1:p.Cys134Tyr
NM_001039848.2:c.512G>A	NP_001034937.1:p.Cys171Tyr
NM_002085.4:c.401G>A	NP_002076.2:p.Cys134Tyr
NM_001039848.3:c.512G>A	NP_001034937.1:p.Cys171Tyr
NM_001039847.3:c.401G>A	NP_001034936.1:p.Cys134Tyr
NM_001039848.4:c.512G>A	NP_001034937.1:p.Cys171Tyr
NM_001367832.1:c.320G>A	NP_001354761.1:p.Cys107Tyr
NM_002085.5:c.401G>A MANE Select	NP_002076.2:p.Cys134Tyr