Canonical Allele Identifier: CA2576545082
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105455dup , CM000681.2:g.1105455dup GRCh38
NC_000019.9:g.1105454dup , CM000681.1:g.1105454dup GRCh37
NC_000019.8:g.1056454dup NCBI36
NG_050621.1:g.6530dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585362.7:c.380dup ENSP00000473614.3:p.Tyr127Ter
ENST00000593032.6:c.188dup ENSP00000465828.4:p.Tyr63Ter
ENST00000706713.1:c.263dup ENSP00000516510.1:p.Tyr88Ter
ENST00000706714.1:c.188dup ENSP00000516511.1:p.Tyr63Ter
ENST00000706715.1:c.-116dup ENSP00000516512.1:n.-116dup
ENST00000354171.13:c.269dup MANE Select ENSP00000346103.7:p.Tyr90Ter
ENST00000589115.6:c.269dup ENSP00000466872.3:p.Tyr90Ter
ENST00000354171.12:c.269dup ENSP00000346103.7:p.Tyr90Ter
ENST00000585362.6:c.380dup ENSP00000473614.2:p.Tyr127Ter
ENST00000585480.1:c.2dup ENSP00000467900.1:p.Tyr1Ter
ENST00000587648.5:c.149dup ENSP00000468349.1:p.Tyr50Ter
ENST00000587932.2:n.203dup
ENST00000588919.5:c.188dup ENSP00000464989.3:p.Tyr63Ter
ENST00000589115.5:c.269dup ENSP00000466872.2:p.Tyr90Ter
ENST00000592940.2:n.215dup
ENST00000593032.5:c.188dup ENSP00000465828.3:p.Tyr63Ter
ENST00000611653.4:c.188dup ENSP00000483655.1:p.Tyr63Ter
ENST00000614791.1:c.374dup ENSP00000484697.1:p.Tyr125Ter
ENST00000616066.4:c.266dup ENSP00000485000.1:p.Tyr89Ter
ENST00000622390.4:c.377dup ENSP00000477503.1:p.Tyr126Ter
NM_001039847.2:c.269dup NP_001034936.1:p.Tyr90Ter
NM_001039848.2:c.380dup NP_001034937.1:p.Tyr127Ter
NM_002085.4:c.269dup NP_002076.2:p.Tyr90Ter
NM_001039848.3:c.380dup NP_001034937.1:p.Tyr127Ter
NM_001039847.3:c.269dup NP_001034936.1:p.Tyr90Ter
NM_001039848.4:c.380dup NP_001034937.1:p.Tyr127Ter
NM_001367832.1:c.188dup NP_001354761.1:p.Tyr63Ter
NM_002085.5:c.269dup MANE Select NP_002076.2:p.Tyr90Ter