Canonical Allele Identifier: CA504693901
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1104082-G-T
MyVariant Identifiers: chr19:g.1104081G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104082G>T , CM000681.2:g.1104082G>T GRCh38
NC_000019.9:g.1104081G>T , CM000681.1:g.1104081G>T GRCh37
NC_000019.8:g.1055081G>T NCBI36
NG_050621.1:g.5157G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000593032.6:c.-43G>T ENSP00000465828.4:n.-43G>T
ENST00000706713.1:c.39G>T ENSP00000516510.1:p.Ala13=
ENST00000706714.1:c.-43G>T ENSP00000516511.1:n.-43G>T
ENST00000354171.13:c.39G>T MANE Select ENSP00000346103.7:p.Ala13=
ENST00000589115.6:c.39G>T ENSP00000466872.3:p.Ala13=
ENST00000354171.12:c.39G>T ENSP00000346103.7:p.Ala13=
ENST00000588919.5:c.-43G>T ENSP00000464989.3:n.-43G>T
ENST00000589115.5:c.39G>T ENSP00000466872.2:p.Ala13=
ENST00000593032.5:c.-43G>T ENSP00000465828.3:n.-43G>T
ENST00000611653.4:c.-43G>T ENSP00000483655.1:n.-43G>T
ENST00000616066.4:c.39G>T ENSP00000485000.1:p.Ala13=
NM_001039847.2:c.39G>T NP_001034936.1:p.Ala13=
NM_002085.4:c.39G>T NP_002076.2:p.Ala13=
NM_001039847.3:c.39G>T NP_001034936.1:p.Ala13=
NM_001367832.1:c.-43G>T NP_001354761.1:n.-43G>T
NM_002085.5:c.39G>T MANE Select NP_002076.2:p.Ala13=