Canonical Allele Identifier: CA2588207862
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106507_1106511del , CM000681.2:g.1106507_1106511del GRCh38
NC_000019.9:g.1106506_1106510del , CM000681.1:g.1106506_1106510del GRCh37
NC_000019.8:g.1057506_1057510del NCBI36
NG_050621.1:g.7582_7586del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.673-33_673-29del ENSP00000473614.3:n.673-33_673-29del
ENST00000593032.6:c.542-33_542-29del ENSP00000465828.4:n.542-33_542-29del
ENST00000706713.1:c.556-33_556-29del ENSP00000516510.1:n.556-33_556-29del
ENST00000706714.1:c.542-33_542-29del ENSP00000516511.1:n.542-33_542-29del
ENST00000706715.1:c.178-33_178-29del ENSP00000516512.1:n.178-33_178-29del
ENST00000354171.13:c.562-33_562-29del MANE Select ENSP00000346103.7:n.562-33_562-29del
ENST00000589115.6:c.537-33_537-29del ENSP00000466872.3:n.537-33_537-29del
ENST00000354171.12:c.562-33_562-29del ENSP00000346103.7:n.562-33_562-29del
ENST00000585480.1:c.294+48_294+52del ENSP00000467900.1:n.294+48_294+52del
ENST00000587648.5:c.442-33_442-29del ENSP00000468349.1:n.442-33_442-29del
ENST00000588919.5:c.503-33_503-29del ENSP00000464989.3:n.503-33_503-29del
ENST00000589115.5:c.537-33_537-29del ENSP00000466872.2:n.537-33_537-29del
ENST00000592940.2:n.933-33_933-29del
ENST00000611653.4:c.481-33_481-29del ENSP00000483655.1:n.481-33_481-29del
ENST00000616066.4:c.559-33_559-29del ENSP00000485000.1:n.559-33_559-29del
ENST00000622390.4:c.670-33_670-29del ENSP00000477503.1:n.670-33_670-29del
NM_001039847.2:c.584-33_584-29del NP_001034936.1:n.584-33_584-29del
NM_001039848.2:c.673-33_673-29del NP_001034937.1:n.673-33_673-29del
NM_002085.4:c.562-33_562-29del NP_002076.2:n.562-33_562-29del
NM_001039848.3:c.673-33_673-29del NP_001034937.1:n.673-33_673-29del
NM_001039847.3:c.584-33_584-29del NP_001034936.1:n.584-33_584-29del
NM_001039848.4:c.673-33_673-29del NP_001034937.1:n.673-33_673-29del
NM_001367832.1:c.481-33_481-29del NP_001354761.1:n.481-33_481-29del
NM_002085.5:c.562-33_562-29del MANE Select NP_002076.2:n.562-33_562-29del