Canonical Allele Identifier: CA9037381
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs762541815

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105858dup , CM000681.2:g.1105858dup GRCh38
NC_000019.9:g.1105857dup , CM000681.1:g.1105857dup GRCh37
NC_000019.8:g.1056857dup NCBI36
NG_050621.1:g.6933dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.587+49dup ENSP00000473614.3:n.587+49dup
ENST00000593032.6:c.395+49dup ENSP00000465828.4:n.395+49dup
ENST00000706713.1:c.470+49dup ENSP00000516510.1:n.470+49dup
ENST00000706714.1:c.395+49dup ENSP00000516511.1:n.395+49dup
ENST00000706715.1:c.92+49dup ENSP00000516512.1:n.92+49dup
ENST00000354171.13:c.476+49dup MANE Select ENSP00000346103.7:n.476+49dup
ENST00000589115.6:c.476+49dup ENSP00000466872.3:n.476+49dup
ENST00000354171.12:c.476+49dup ENSP00000346103.7:n.476+49dup
ENST00000585480.1:c.209+49dup ENSP00000467900.1:n.209+49dup
ENST00000587648.5:c.356+49dup ENSP00000468349.1:n.356+49dup
ENST00000588919.5:c.395+49dup ENSP00000464989.3:n.395+49dup
ENST00000589115.5:c.476+49dup ENSP00000466872.2:n.476+49dup
ENST00000592940.2:n.464dup
ENST00000593032.5:c.395+49dup ENSP00000465828.3:n.395+49dup
ENST00000611653.4:c.395+49dup ENSP00000483655.1:n.395+49dup
ENST00000616066.4:c.473+49dup ENSP00000485000.1:n.473+49dup
ENST00000622390.4:c.584+49dup ENSP00000477503.1:n.584+49dup
NM_001039847.2:c.476+49dup NP_001034936.1:n.476+49dup
NM_001039848.2:c.587+49dup NP_001034937.1:n.587+49dup
NM_002085.4:c.476+49dup NP_002076.2:n.476+49dup
NM_001039848.3:c.587+49dup NP_001034937.1:n.587+49dup
NM_001039847.3:c.476+49dup NP_001034936.1:n.476+49dup
NM_001039848.4:c.587+49dup NP_001034937.1:n.587+49dup
NM_001367832.1:c.395+49dup NP_001354761.1:n.395+49dup
NM_002085.5:c.476+49dup MANE Select NP_002076.2:n.476+49dup