Canonical Allele Identifier: CA303995193

Gene: GPX4

Linked Data

• dbSNP Id: rs1046937374
• gnomAD v2: 19-1106528-C-T
• gnomAD v3: 19-1106529-C-T
• gnomAD v4: 19-1106529-C-T
• MyVariant Identifiers: chr19:g.1106528C>T (hg19) ; chr19:g.1106529C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106529C>T , CM000681.2:g.1106529C>T	GRCh38
NC_000019.9:g.1106528C>T , CM000681.1:g.1106528C>T	GRCh37
NC_000019.8:g.1057528C>T	NCBI36
NG_050621.1:g.7604C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.673-11C>T	ENSP00000473614.3:n.673-11C>T
ENST00000593032.6:c.542-11C>T	ENSP00000465828.4:n.542-11C>T
ENST00000706713.1:c.556-11C>T	ENSP00000516510.1:n.556-11C>T
ENST00000706714.1:c.542-11C>T	ENSP00000516511.1:n.542-11C>T
ENST00000706715.1:c.178-11C>T	ENSP00000516512.1:n.178-11C>T
ENST00000354171.13:c.562-11C>T MANE Select	ENSP00000346103.7:n.562-11C>T
ENST00000589115.6:c.537-11C>T	ENSP00000466872.3:n.537-11C>T
ENST00000354171.12:c.562-11C>T	ENSP00000346103.7:n.562-11C>T
ENST00000585480.1:c.295-44C>T	ENSP00000467900.1:n.295-44C>T
ENST00000587648.5:c.442-11C>T	ENSP00000468349.1:n.442-11C>T
ENST00000588919.5:c.503-11C>T	ENSP00000464989.3:n.503-11C>T
ENST00000589115.5:c.537-11C>T	ENSP00000466872.2:n.537-11C>T
ENST00000592940.2:n.933-11C>T
ENST00000611653.4:c.481-11C>T	ENSP00000483655.1:n.481-11C>T
ENST00000616066.4:c.559-11C>T	ENSP00000485000.1:n.559-11C>T
ENST00000622390.4:c.670-11C>T	ENSP00000477503.1:n.670-11C>T
NM_001039847.2:c.584-11C>T	NP_001034936.1:n.584-11C>T
NM_001039848.2:c.673-11C>T	NP_001034937.1:n.673-11C>T
NM_002085.4:c.562-11C>T	NP_002076.2:n.562-11C>T
NM_001039848.3:c.673-11C>T	NP_001034937.1:n.673-11C>T
NM_001039847.3:c.584-11C>T	NP_001034936.1:n.584-11C>T
NM_001039848.4:c.673-11C>T	NP_001034937.1:n.673-11C>T
NM_001367832.1:c.481-11C>T	NP_001354761.1:n.481-11C>T
NM_002085.5:c.562-11C>T MANE Select	NP_002076.2:n.562-11C>T