Canonical Allele Identifier: CA2576544969
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104003_1104006dup , CM000681.2:g.1104003_1104006dup GRCh38
NC_000019.9:g.1104002_1104005dup , CM000681.1:g.1104002_1104005dup GRCh37
NC_000019.8:g.1055002_1055005dup NCBI36
NG_050621.1:g.5078_5081dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-41_-38dup ENSP00000516510.1:n.-41_-38dup
ENST00000354171.13:c.-41_-38dup MANE Select ENSP00000346103.7:n.-41_-38dup
ENST00000354171.12:c.-41_-38dup ENSP00000346103.7:n.-41_-38dup
ENST00000616066.4:c.-41_-38dup ENSP00000485000.1:n.-41_-38dup
NM_001039847.2:c.-41_-38dup NP_001034936.1:n.-41_-38dup
NM_002085.4:c.-41_-38dup NP_002076.2:n.-41_-38dup
NM_001039847.3:c.-41_-38dup NP_001034936.1:n.-41_-38dup
NM_002085.5:c.-41_-38dup MANE Select NP_002076.2:n.-41_-38dup