Canonical Allele Identifier: CA402940797

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106761A>T (hg19) ; chr19:g.1106762A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106762A>T , CM000681.2:g.1106762A>T	GRCh38
NC_000019.9:g.1106761A>T , CM000681.1:g.1106761A>T	GRCh37
NC_000019.8:g.1057761A>T	NCBI36
NG_050621.1:g.7837A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*190A>T	ENSP00000473614.3:n.*190A>T
ENST00000593032.6:c.764A>T	ENSP00000465828.4:p.Glu255Val
ENST00000706713.1:c.*190A>T	ENSP00000516510.1:n.*190A>T
ENST00000706714.1:c.764A>T	ENSP00000516511.1:p.Glu255Val
ENST00000706715.1:c.*190A>T	ENSP00000516512.1:n.*190A>T
ENST00000354171.13:c.*190A>T MANE Select	ENSP00000346103.7:n.*190A>T
ENST00000589115.6:c.*216A>T	ENSP00000466872.3:n.*216A>T
ENST00000354171.12:c.*190A>T	ENSP00000346103.7:n.*190A>T
ENST00000585480.1:c.484A>T	ENSP00000467900.1:p.Asn162Tyr
ENST00000588919.5:c.725A>T	ENSP00000464989.3:p.Glu242Val
ENST00000589115.5:c.*216A>T	ENSP00000466872.2:n.*216A>T
ENST00000592940.2:n.1155A>T
ENST00000611653.4:c.*190A>T	ENSP00000483655.1:n.*190A>T
ENST00000616066.4:c.*190A>T	ENSP00000485000.1:n.*190A>T
ENST00000622390.4:c.*190A>T	ENSP00000477503.1:n.*190A>T
NM_001039847.2:c.*122A>T	NP_001034936.1:n.*122A>T
NM_001039848.2:c.*190A>T	NP_001034937.1:n.*190A>T
NM_002085.4:c.*190A>T	NP_002076.2:n.*190A>T
NM_001039848.3:c.*190A>T	NP_001034937.1:n.*190A>T
NM_001039847.3:c.*122A>T	NP_001034936.1:n.*122A>T
NM_001039848.4:c.*190A>T	NP_001034937.1:n.*190A>T
NM_001367832.1:c.*190A>T	NP_001354761.1:n.*190A>T
NM_002085.5:c.*190A>T MANE Select	NP_002076.2:n.*190A>T