Canonical Allele Identifier: CA9037301
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs8178973

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105623dup , CM000681.2:g.1105623dup GRCh38
NC_000019.9:g.1105622dup , CM000681.1:g.1105622dup GRCh37
NC_000019.8:g.1056622dup NCBI36
NG_050621.1:g.6698dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.436-35dup ENSP00000473614.3:n.436-35dup
ENST00000593032.6:c.244-35dup ENSP00000465828.4:n.244-35dup
ENST00000706713.1:c.319-35dup ENSP00000516510.1:n.319-35dup
ENST00000706714.1:c.244-35dup ENSP00000516511.1:n.244-35dup
ENST00000706715.1:c.-60-35dup ENSP00000516512.1:n.-60-35dup
ENST00000354171.13:c.325-35dup MANE Select ENSP00000346103.7:n.325-35dup
ENST00000589115.6:c.325-35dup ENSP00000466872.3:n.325-35dup
ENST00000354171.12:c.325-35dup ENSP00000346103.7:n.325-35dup
ENST00000585362.6:c.436-35dup ENSP00000473614.2:n.436-35dup
ENST00000585480.1:c.58-35dup ENSP00000467900.1:n.58-35dup
ENST00000587648.5:c.205-35dup ENSP00000468349.1:n.205-35dup
ENST00000587932.2:n.259-35dup
ENST00000588919.5:c.244-35dup ENSP00000464989.3:n.244-35dup
ENST00000589115.5:c.325-35dup ENSP00000466872.2:n.325-35dup
ENST00000592940.2:n.271-42dup
ENST00000593032.5:c.244-35dup ENSP00000465828.3:n.244-35dup
ENST00000611653.4:c.244-35dup ENSP00000483655.1:n.244-35dup
ENST00000616066.4:c.322-35dup ENSP00000485000.1:n.322-35dup
ENST00000622390.4:c.433-35dup ENSP00000477503.1:n.433-35dup
NM_001039847.2:c.325-35dup NP_001034936.1:n.325-35dup
NM_001039848.2:c.436-35dup NP_001034937.1:n.436-35dup
NM_002085.4:c.325-35dup NP_002076.2:n.325-35dup
NM_001039848.3:c.436-35dup NP_001034937.1:n.436-35dup
NM_001039847.3:c.325-35dup NP_001034936.1:n.325-35dup
NM_001039848.4:c.436-35dup NP_001034937.1:n.436-35dup
NM_001367832.1:c.244-35dup NP_001354761.1:n.244-35dup
NM_002085.5:c.325-35dup MANE Select NP_002076.2:n.325-35dup