Canonical Allele Identifier: CA2582332178
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2145164038

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104080dup , CM000681.2:g.1104080dup GRCh38
NC_000019.9:g.1104079dup , CM000681.1:g.1104079dup GRCh37
NC_000019.8:g.1055079dup NCBI36
NG_050621.1:g.5155dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000593032.6:c.-45dup ENSP00000465828.4:n.-45dup
ENST00000706713.1:c.37dup ENSP00000516510.1:p.Ala13GlyfsTer?
ENST00000706714.1:c.-45dup ENSP00000516511.1:n.-45dup
ENST00000354171.13:c.37dup MANE Select ENSP00000346103.7:p.Ala13GlyfsTer?
ENST00000589115.6:c.37dup ENSP00000466872.3:p.Ala13GlyfsTer?
ENST00000354171.12:c.37dup ENSP00000346103.7:p.Ala13GlyfsTer?
ENST00000588919.5:c.-45dup ENSP00000464989.3:n.-45dup
ENST00000589115.5:c.37dup ENSP00000466872.2:p.Ala13GlyfsTer?
ENST00000593032.5:c.-45dup ENSP00000465828.3:n.-45dup
ENST00000611653.4:c.-45dup ENSP00000483655.1:n.-45dup
ENST00000616066.4:c.37dup ENSP00000485000.1:p.Ala13GlyfsTer?
NM_001039847.2:c.37dup NP_001034936.1:p.Ala13GlyfsTer?
NM_002085.4:c.37dup NP_002076.2:p.Ala13GlyfsTer?
NM_001039847.3:c.37dup NP_001034936.1:p.Ala13GlyfsTer?
NM_001367832.1:c.-45dup NP_001354761.1:n.-45dup
NM_002085.5:c.37dup MANE Select NP_002076.2:p.Ala13GlyfsTer?