Canonical Allele Identifier: CA2317520006

Gene: GPX4

Linked Data

• dbSNP Id: rs1366069298
• gnomAD v4: 19-1105581-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105581G>A , CM000681.2:g.1105581G>A	GRCh38
NC_000019.9:g.1105580G>A , CM000681.1:g.1105580G>A	GRCh37
NC_000019.8:g.1056580G>A	NCBI36
NG_050621.1:g.6656G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.435+71G>A	ENSP00000473614.3:n.435+71G>A
ENST00000593032.6:c.243+71G>A	ENSP00000465828.4:n.243+71G>A
ENST00000706713.1:c.318+71G>A	ENSP00000516510.1:n.318+71G>A
ENST00000706714.1:c.243+71G>A	ENSP00000516511.1:n.243+71G>A
ENST00000706715.1:c.-61+71G>A	ENSP00000516512.1:n.-61+71G>A
ENST00000354171.13:c.324+71G>A MANE Select	ENSP00000346103.7:n.324+71G>A
ENST00000589115.6:c.324+71G>A	ENSP00000466872.3:n.324+71G>A
ENST00000354171.12:c.324+71G>A	ENSP00000346103.7:n.324+71G>A
ENST00000585362.6:c.435+71G>A	ENSP00000473614.2:n.435+71G>A
ENST00000585480.1:c.57+71G>A	ENSP00000467900.1:n.57+71G>A
ENST00000587648.5:c.204+71G>A	ENSP00000468349.1:n.204+71G>A
ENST00000587932.2:n.258+71G>A
ENST00000588919.5:c.243+71G>A	ENSP00000464989.3:n.243+71G>A
ENST00000589115.5:c.324+71G>A	ENSP00000466872.2:n.324+71G>A
ENST00000592940.2:n.270+71G>A
ENST00000593032.5:c.243+71G>A	ENSP00000465828.3:n.243+71G>A
ENST00000611653.4:c.243+71G>A	ENSP00000483655.1:n.243+71G>A
ENST00000616066.4:c.321+71G>A	ENSP00000485000.1:n.321+71G>A
ENST00000622390.4:c.432+71G>A	ENSP00000477503.1:n.432+71G>A
NM_001039847.2:c.324+71G>A	NP_001034936.1:n.324+71G>A
NM_001039848.2:c.435+71G>A	NP_001034937.1:n.435+71G>A
NM_002085.4:c.324+71G>A	NP_002076.2:n.324+71G>A
NM_001039848.3:c.435+71G>A	NP_001034937.1:n.435+71G>A
NM_001039847.3:c.324+71G>A	NP_001034936.1:n.324+71G>A
NM_001039848.4:c.435+71G>A	NP_001034937.1:n.435+71G>A
NM_001367832.1:c.243+71G>A	NP_001354761.1:n.243+71G>A
NM_002085.5:c.324+71G>A MANE Select	NP_002076.2:n.324+71G>A