Canonical Allele Identifier: CA2588205771
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1103999-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103999T>A , CM000681.2:g.1103999T>A GRCh38
NC_000019.9:g.1103998T>A , CM000681.1:g.1103998T>A GRCh37
NC_000019.8:g.1054998T>A NCBI36
NG_050621.1:g.5074T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-45T>A ENSP00000516510.1:n.-45T>A
ENST00000354171.13:c.-45T>A MANE Select ENSP00000346103.7:n.-45T>A
ENST00000354171.12:c.-45T>A ENSP00000346103.7:n.-45T>A
ENST00000616066.4:c.-45T>A ENSP00000485000.1:n.-45T>A
NM_001039847.2:c.-45T>A NP_001034936.1:n.-45T>A
NM_002085.4:c.-45T>A NP_002076.2:n.-45T>A
NM_001039847.3:c.-45T>A NP_001034936.1:n.-45T>A
NM_002085.5:c.-45T>A MANE Select NP_002076.2:n.-45T>A
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