Canonical Allele Identifier: CA631298766

Gene: GPX4

Linked Data

• dbSNP Id: rs1018762954
• gnomAD v2: 19-1105626-C-G
• gnomAD v4: 19-1105627-C-G
• MyVariant Identifiers: chr19:g.1105626C>G (hg19) ; chr19:g.1105627C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105627C>G , CM000681.2:g.1105627C>G	GRCh38
NC_000019.9:g.1105626C>G , CM000681.1:g.1105626C>G	GRCh37
NC_000019.8:g.1056626C>G	NCBI36
NG_050621.1:g.6702C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.436-31C>G	ENSP00000473614.3:n.436-31C>G
ENST00000593032.6:c.244-31C>G	ENSP00000465828.4:n.244-31C>G
ENST00000706713.1:c.319-31C>G	ENSP00000516510.1:n.319-31C>G
ENST00000706714.1:c.244-31C>G	ENSP00000516511.1:n.244-31C>G
ENST00000706715.1:c.-60-31C>G	ENSP00000516512.1:n.-60-31C>G
ENST00000354171.13:c.325-31C>G MANE Select	ENSP00000346103.7:n.325-31C>G
ENST00000589115.6:c.325-31C>G	ENSP00000466872.3:n.325-31C>G
ENST00000354171.12:c.325-31C>G	ENSP00000346103.7:n.325-31C>G
ENST00000585362.6:c.436-31C>G	ENSP00000473614.2:n.436-31C>G
ENST00000585480.1:c.58-31C>G	ENSP00000467900.1:n.58-31C>G
ENST00000587648.5:c.205-31C>G	ENSP00000468349.1:n.205-31C>G
ENST00000587932.2:n.259-31C>G
ENST00000588919.5:c.244-31C>G	ENSP00000464989.3:n.244-31C>G
ENST00000589115.5:c.325-31C>G	ENSP00000466872.2:n.325-31C>G
ENST00000592940.2:n.271-38C>G
ENST00000593032.5:c.244-31C>G	ENSP00000465828.3:n.244-31C>G
ENST00000611653.4:c.244-31C>G	ENSP00000483655.1:n.244-31C>G
ENST00000616066.4:c.322-31C>G	ENSP00000485000.1:n.322-31C>G
ENST00000622390.4:c.433-31C>G	ENSP00000477503.1:n.433-31C>G
NM_001039847.2:c.325-31C>G	NP_001034936.1:n.325-31C>G
NM_001039848.2:c.436-31C>G	NP_001034937.1:n.436-31C>G
NM_002085.4:c.325-31C>G	NP_002076.2:n.325-31C>G
NM_001039848.3:c.436-31C>G	NP_001034937.1:n.436-31C>G
NM_001039847.3:c.325-31C>G	NP_001034936.1:n.325-31C>G
NM_001039848.4:c.436-31C>G	NP_001034937.1:n.436-31C>G
NM_001367832.1:c.244-31C>G	NP_001354761.1:n.244-31C>G
NM_002085.5:c.325-31C>G MANE Select	NP_002076.2:n.325-31C>G