Canonical Allele Identifier: CA2813238405
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105557_1105558insGGGGG , CM000681.2:g.1105557_1105558insGGGGG GRCh38
NC_000019.9:g.1105556_1105557insGGGGG , CM000681.1:g.1105556_1105557insGGGGG GRCh37
NC_000019.8:g.1056556_1056557insGGGGG NCBI36
NG_050621.1:g.6632_6633insGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.435+47_435+48insGGGGG ENSP00000473614.3:n.435+47_435+48insGGGGG
ENST00000593032.6:c.243+47_243+48insGGGGG ENSP00000465828.4:n.243+47_243+48insGGGGG
ENST00000706713.1:c.318+47_318+48insGGGGG ENSP00000516510.1:n.318+47_318+48insGGGGG
ENST00000706714.1:c.243+47_243+48insGGGGG ENSP00000516511.1:n.243+47_243+48insGGGGG
ENST00000706715.1:c.-61+47_-61+48insGGGGG ENSP00000516512.1:n.-61+47_-61+48insGGGGG
ENST00000354171.13:c.324+47_324+48insGGGGG MANE Select ENSP00000346103.7:n.324+47_324+48insGGGGG
ENST00000589115.6:c.324+47_324+48insGGGGG ENSP00000466872.3:n.324+47_324+48insGGGGG
ENST00000354171.12:c.324+47_324+48insGGGGG ENSP00000346103.7:n.324+47_324+48insGGGGG
ENST00000585362.6:c.435+47_435+48insGGGGG ENSP00000473614.2:n.435+47_435+48insGGGGG
ENST00000585480.1:c.57+47_57+48insGGGGG ENSP00000467900.1:n.57+47_57+48insGGGGG
ENST00000587648.5:c.204+47_204+48insGGGGG ENSP00000468349.1:n.204+47_204+48insGGGGG
ENST00000587932.2:n.258+47_258+48insGGGGG
ENST00000588919.5:c.243+47_243+48insGGGGG ENSP00000464989.3:n.243+47_243+48insGGGGG
ENST00000589115.5:c.324+47_324+48insGGGGG ENSP00000466872.2:n.324+47_324+48insGGGGG
ENST00000592940.2:n.270+47_270+48insGGGGG
ENST00000593032.5:c.243+47_243+48insGGGGG ENSP00000465828.3:n.243+47_243+48insGGGGG
ENST00000611653.4:c.243+47_243+48insGGGGG ENSP00000483655.1:n.243+47_243+48insGGGGG
ENST00000616066.4:c.321+47_321+48insGGGGG ENSP00000485000.1:n.321+47_321+48insGGGGG
ENST00000622390.4:c.432+47_432+48insGGGGG ENSP00000477503.1:n.432+47_432+48insGGGGG
NM_001039847.2:c.324+47_324+48insGGGGG NP_001034936.1:n.324+47_324+48insGGGGG
NM_001039848.2:c.435+47_435+48insGGGGG NP_001034937.1:n.435+47_435+48insGGGGG
NM_002085.4:c.324+47_324+48insGGGGG NP_002076.2:n.324+47_324+48insGGGGG
NM_001039848.3:c.435+47_435+48insGGGGG NP_001034937.1:n.435+47_435+48insGGGGG
NM_001039847.3:c.324+47_324+48insGGGGG NP_001034936.1:n.324+47_324+48insGGGGG
NM_001039848.4:c.435+47_435+48insGGGGG NP_001034937.1:n.435+47_435+48insGGGGG
NM_001367832.1:c.243+47_243+48insGGGGG NP_001354761.1:n.243+47_243+48insGGGGG
NM_002085.5:c.324+47_324+48insGGGGG MANE Select NP_002076.2:n.324+47_324+48insGGGGG