Canonical Allele Identifier: CA402939152

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106249A>T (hg19) ; chr19:g.1106250A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106250A>T , CM000681.2:g.1106250A>T	GRCh38
NC_000019.9:g.1106249A>T , CM000681.1:g.1106249A>T	GRCh37
NC_000019.8:g.1057249A>T	NCBI36
NG_050621.1:g.7325A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.596A>T	ENSP00000473614.3:p.Lys199Met
ENST00000593032.6:c.465A>T	ENSP00000465828.4:p.Gln155His
ENST00000706713.1:c.479A>T	ENSP00000516510.1:p.Lys160Met
ENST00000706714.1:c.465A>T	ENSP00000516511.1:p.Gln155His
ENST00000706715.1:c.101A>T	ENSP00000516512.1:p.Lys34Met
ENST00000354171.13:c.485A>T MANE Select	ENSP00000346103.7:p.Lys162Met
ENST00000589115.6:c.477-150A>T	ENSP00000466872.3:n.477-150A>T
ENST00000354171.12:c.485A>T	ENSP00000346103.7:p.Lys162Met
ENST00000585480.1:c.218A>T	ENSP00000467900.1:p.Lys73Met
ENST00000587648.5:c.365A>T	ENSP00000468349.1:p.Lys122Met
ENST00000588919.5:c.404A>T	ENSP00000464989.3:p.Lys135Met
ENST00000589115.5:c.477-150A>T	ENSP00000466872.2:n.477-150A>T
ENST00000592940.2:n.856A>T
ENST00000593032.5:c.465A>T	ENSP00000465828.3:p.Gln155His
ENST00000611653.4:c.404A>T	ENSP00000483655.1:p.Lys135Met
ENST00000616066.4:c.482A>T	ENSP00000485000.1:p.Lys161Met
ENST00000622390.4:c.593A>T	ENSP00000477503.1:p.Lys198Met
NM_001039847.2:c.485A>T	NP_001034936.1:p.Lys162Met
NM_001039848.2:c.596A>T	NP_001034937.1:p.Lys199Met
NM_002085.4:c.485A>T	NP_002076.2:p.Lys162Met
NM_001039848.3:c.596A>T	NP_001034937.1:p.Lys199Met
NM_001039847.3:c.485A>T	NP_001034936.1:p.Lys162Met
NM_001039848.4:c.596A>T	NP_001034937.1:p.Lys199Met
NM_001367832.1:c.404A>T	NP_001354761.1:p.Lys135Met
NM_002085.5:c.485A>T MANE Select	NP_002076.2:p.Lys162Met