Canonical Allele Identifier: CA402934210
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1163055709
gnomAD v2: 19-1104083-T-C
gnomAD v4: 19-1104084-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104084T>C , CM000681.2:g.1104084T>C GRCh38
NC_000019.9:g.1104083T>C , CM000681.1:g.1104083T>C GRCh37
NC_000019.8:g.1055083T>C NCBI36
NG_050621.1:g.5159T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000593032.6:c.-41T>C ENSP00000465828.4:n.-41T>C
ENST00000706713.1:c.41T>C ENSP00000516510.1:p.Leu14Pro
ENST00000706714.1:c.-41T>C ENSP00000516511.1:n.-41T>C
ENST00000354171.13:c.41T>C MANE Select ENSP00000346103.7:p.Leu14Pro
ENST00000589115.6:c.41T>C ENSP00000466872.3:p.Leu14Pro
ENST00000354171.12:c.41T>C ENSP00000346103.7:p.Leu14Pro
ENST00000588919.5:c.-41T>C ENSP00000464989.3:n.-41T>C
ENST00000589115.5:c.41T>C ENSP00000466872.2:p.Leu14Pro
ENST00000593032.5:c.-41T>C ENSP00000465828.3:n.-41T>C
ENST00000611653.4:c.-41T>C ENSP00000483655.1:n.-41T>C
ENST00000616066.4:c.41T>C ENSP00000485000.1:p.Leu14Pro
NM_001039847.2:c.41T>C NP_001034936.1:p.Leu14Pro
NM_002085.4:c.41T>C NP_002076.2:p.Leu14Pro
NM_001039847.3:c.41T>C NP_001034936.1:p.Leu14Pro
NM_001367832.1:c.-41T>C NP_001354761.1:n.-41T>C
NM_002085.5:c.41T>C MANE Select NP_002076.2:p.Leu14Pro