Canonical Allele Identifier: CA402937174
Gene: GPX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1105455C>G (hg19) chr19:g.1105456C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105456C>G , CM000681.2:g.1105456C>G GRCh38
NC_000019.9:g.1105455C>G , CM000681.1:g.1105455C>G GRCh37
NC_000019.8:g.1056455C>G NCBI36
NG_050621.1:g.6531C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000585362.7:c.381C>G ENSP00000473614.3:p.Tyr127Ter
ENST00000593032.6:c.189C>G ENSP00000465828.4:p.Tyr63Ter
ENST00000706713.1:c.264C>G ENSP00000516510.1:p.Tyr88Ter
ENST00000706714.1:c.189C>G ENSP00000516511.1:p.Tyr63Ter
ENST00000706715.1:c.-115C>G ENSP00000516512.1:n.-115C>G
ENST00000354171.13:c.270C>G MANE Select ENSP00000346103.7:p.Tyr90Ter
ENST00000589115.6:c.270C>G ENSP00000466872.3:p.Tyr90Ter
ENST00000354171.12:c.270C>G ENSP00000346103.7:p.Tyr90Ter
ENST00000585362.6:c.381C>G ENSP00000473614.2:p.Tyr127Ter
ENST00000585480.1:c.3C>G ENSP00000467900.1:p.Tyr1Ter
ENST00000587648.5:c.150C>G ENSP00000468349.1:p.Tyr50Ter
ENST00000587932.2:n.204C>G
ENST00000588919.5:c.189C>G ENSP00000464989.3:p.Tyr63Ter
ENST00000589115.5:c.270C>G ENSP00000466872.2:p.Tyr90Ter
ENST00000592940.2:n.216C>G
ENST00000593032.5:c.189C>G ENSP00000465828.3:p.Tyr63Ter
ENST00000611653.4:c.189C>G ENSP00000483655.1:p.Tyr63Ter
ENST00000614791.1:c.375C>G ENSP00000484697.1:p.Tyr125Ter
ENST00000616066.4:c.267C>G ENSP00000485000.1:p.Tyr89Ter
ENST00000622390.4:c.378C>G ENSP00000477503.1:p.Tyr126Ter
NM_001039847.2:c.270C>G NP_001034936.1:p.Tyr90Ter
NM_001039848.2:c.381C>G NP_001034937.1:p.Tyr127Ter
NM_002085.4:c.270C>G NP_002076.2:p.Tyr90Ter
NM_001039848.3:c.381C>G NP_001034937.1:p.Tyr127Ter
NM_001039847.3:c.270C>G NP_001034936.1:p.Tyr90Ter
NM_001039848.4:c.381C>G NP_001034937.1:p.Tyr127Ter
NM_001367832.1:c.189C>G NP_001354761.1:p.Tyr63Ter
NM_002085.5:c.270C>G MANE Select NP_002076.2:p.Tyr90Ter
Search 100 bp 5'
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