Canonical Allele Identifier: CA402939777

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106412A>T (hg19) ; chr19:g.1106413A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106413A>T , CM000681.2:g.1106413A>T	GRCh38
NC_000019.9:g.1106412A>T , CM000681.1:g.1106412A>T	GRCh37
NC_000019.8:g.1057412A>T	NCBI36
NG_050621.1:g.7488A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.626A>T	ENSP00000473614.3:p.Lys209Met
ENST00000593032.6:c.495A>T	ENSP00000465828.4:p.Gln165His
ENST00000706713.1:c.509A>T	ENSP00000516510.1:p.Lys170Met
ENST00000706714.1:c.495A>T	ENSP00000516511.1:p.Gln165His
ENST00000706715.1:c.131A>T	ENSP00000516512.1:p.Lys44Met
ENST00000354171.13:c.515A>T MANE Select	ENSP00000346103.7:p.Lys172Met
ENST00000589115.6:c.490A>T	ENSP00000466872.3:p.Arg164Ter
ENST00000354171.12:c.515A>T	ENSP00000346103.7:p.Lys172Met
ENST00000585480.1:c.248A>T	ENSP00000467900.1:p.Lys83Met
ENST00000587648.5:c.395A>T	ENSP00000468349.1:p.Lys132Met
ENST00000588919.5:c.456A>T	ENSP00000464989.3:p.Gln152His
ENST00000589115.5:c.490A>T	ENSP00000466872.2:p.Arg164Ter
ENST00000592940.2:n.886A>T
ENST00000593032.5:c.495A>T	ENSP00000465828.3:p.Gln165His
ENST00000611653.4:c.434A>T	ENSP00000483655.1:p.Lys145Met
ENST00000616066.4:c.512A>T	ENSP00000485000.1:p.Lys171Met
ENST00000622390.4:c.623A>T	ENSP00000477503.1:p.Lys208Met
NM_001039847.2:c.537A>T	NP_001034936.1:p.Gln179His
NM_001039848.2:c.626A>T	NP_001034937.1:p.Lys209Met
NM_002085.4:c.515A>T	NP_002076.2:p.Lys172Met
NM_001039848.3:c.626A>T	NP_001034937.1:p.Lys209Met
NM_001039847.3:c.537A>T	NP_001034936.1:p.Gln179His
NM_001039848.4:c.626A>T	NP_001034937.1:p.Lys209Met
NM_001367832.1:c.434A>T	NP_001354761.1:p.Lys145Met
NM_002085.5:c.515A>T MANE Select	NP_002076.2:p.Lys172Met