Canonical Allele Identifier: CA9037464

Gene: GPX4

Linked Data

• dbSNP Id: rs745797291
• ExAC: 19:1106407 C / G
• gnomAD v2: 19-1106407-C-G
• gnomAD v4: 19-1106408-C-G
• MyVariant Identifiers: chr19:g.1106407C>G (hg19) ; chr19:g.1106408C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106408C>G , CM000681.2:g.1106408C>G	GRCh38
NC_000019.9:g.1106407C>G , CM000681.1:g.1106407C>G	GRCh37
NC_000019.8:g.1057407C>G	NCBI36
NG_050621.1:g.7483C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.621C>G	ENSP00000473614.3:p.Ile207Met
ENST00000593032.6:c.490C>G	ENSP00000465828.4:p.Arg164Gly
ENST00000706713.1:c.504C>G	ENSP00000516510.1:p.Ile168Met
ENST00000706714.1:c.490C>G	ENSP00000516511.1:p.Arg164Gly
ENST00000706715.1:c.126C>G	ENSP00000516512.1:p.Ile42Met
ENST00000354171.13:c.510C>G MANE Select	ENSP00000346103.7:p.Ile170Met
ENST00000589115.6:c.485C>G	ENSP00000466872.3:p.Ser162Trp
ENST00000354171.12:c.510C>G	ENSP00000346103.7:p.Ile170Met
ENST00000585480.1:c.243C>G	ENSP00000467900.1:p.Ile81Met
ENST00000587648.5:c.390C>G	ENSP00000468349.1:p.Ile130Met
ENST00000588919.5:c.451C>G	ENSP00000464989.3:p.Arg151Gly
ENST00000589115.5:c.485C>G	ENSP00000466872.2:p.Ser162Trp
ENST00000592940.2:n.881C>G
ENST00000593032.5:c.490C>G	ENSP00000465828.3:p.Arg164Gly
ENST00000611653.4:c.429C>G	ENSP00000483655.1:p.Ile143Met
ENST00000616066.4:c.507C>G	ENSP00000485000.1:p.Ile169Met
ENST00000622390.4:c.618C>G	ENSP00000477503.1:p.Ile206Met
NM_001039847.2:c.532C>G	NP_001034936.1:p.Arg178Gly
NM_001039848.2:c.621C>G	NP_001034937.1:p.Ile207Met
NM_002085.4:c.510C>G	NP_002076.2:p.Ile170Met
NM_001039848.3:c.621C>G	NP_001034937.1:p.Ile207Met
NM_001039847.3:c.532C>G	NP_001034936.1:p.Arg178Gly
NM_001039848.4:c.621C>G	NP_001034937.1:p.Ile207Met
NM_001367832.1:c.429C>G	NP_001354761.1:p.Ile143Met
NM_002085.5:c.510C>G MANE Select	NP_002076.2:p.Ile170Met