Canonical Allele Identifier: CA9037300

Gene: GPX4

Linked Data

• dbSNP Id: rs749509892
• ExAC: 19:1105616 G / A
• gnomAD v2: 19-1105616-G-A
• gnomAD v4: 19-1105617-G-A
• MyVariant Identifiers: chr19:g.1105616G>A (hg19) ; chr19:g.1105617G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105617G>A , CM000681.2:g.1105617G>A	GRCh38
NC_000019.9:g.1105616G>A , CM000681.1:g.1105616G>A	GRCh37
NC_000019.8:g.1056616G>A	NCBI36
NG_050621.1:g.6692G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.436-41G>A	ENSP00000473614.3:n.436-41G>A
ENST00000593032.6:c.244-41G>A	ENSP00000465828.4:n.244-41G>A
ENST00000706713.1:c.319-41G>A	ENSP00000516510.1:n.319-41G>A
ENST00000706714.1:c.244-41G>A	ENSP00000516511.1:n.244-41G>A
ENST00000706715.1:c.-60-41G>A	ENSP00000516512.1:n.-60-41G>A
ENST00000354171.13:c.325-41G>A MANE Select	ENSP00000346103.7:n.325-41G>A
ENST00000589115.6:c.325-41G>A	ENSP00000466872.3:n.325-41G>A
ENST00000354171.12:c.325-41G>A	ENSP00000346103.7:n.325-41G>A
ENST00000585362.6:c.436-41G>A	ENSP00000473614.2:n.436-41G>A
ENST00000585480.1:c.58-41G>A	ENSP00000467900.1:n.58-41G>A
ENST00000587648.5:c.205-41G>A	ENSP00000468349.1:n.205-41G>A
ENST00000587932.2:n.259-41G>A
ENST00000588919.5:c.244-41G>A	ENSP00000464989.3:n.244-41G>A
ENST00000589115.5:c.325-41G>A	ENSP00000466872.2:n.325-41G>A
ENST00000592940.2:n.271-48G>A
ENST00000593032.5:c.244-41G>A	ENSP00000465828.3:n.244-41G>A
ENST00000611653.4:c.244-41G>A	ENSP00000483655.1:n.244-41G>A
ENST00000616066.4:c.322-41G>A	ENSP00000485000.1:n.322-41G>A
ENST00000622390.4:c.433-41G>A	ENSP00000477503.1:n.433-41G>A
NM_001039847.2:c.325-41G>A	NP_001034936.1:n.325-41G>A
NM_001039848.2:c.436-41G>A	NP_001034937.1:n.436-41G>A
NM_002085.4:c.325-41G>A	NP_002076.2:n.325-41G>A
NM_001039848.3:c.436-41G>A	NP_001034937.1:n.436-41G>A
NM_001039847.3:c.325-41G>A	NP_001034936.1:n.325-41G>A
NM_001039848.4:c.436-41G>A	NP_001034937.1:n.436-41G>A
NM_001367832.1:c.244-41G>A	NP_001354761.1:n.244-41G>A
NM_002085.5:c.325-41G>A MANE Select	NP_002076.2:n.325-41G>A