Canonical Allele Identifier: CA504694659

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105780-C-A
• MyVariant Identifiers: chr19:g.1105779C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105780C>A , CM000681.2:g.1105780C>A	GRCh38
NC_000019.9:g.1105779C>A , CM000681.1:g.1105779C>A	GRCh37
NC_000019.8:g.1056779C>A	NCBI36
NG_050621.1:g.6855C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.558C>A	ENSP00000473614.3:p.Ile186=
ENST00000593032.6:c.366C>A	ENSP00000465828.4:p.Ile122=
ENST00000706713.1:c.441C>A	ENSP00000516510.1:p.Ile147=
ENST00000706714.1:c.366C>A	ENSP00000516511.1:p.Ile122=
ENST00000706715.1:c.63C>A	ENSP00000516512.1:p.Ile21=
ENST00000354171.13:c.447C>A MANE Select	ENSP00000346103.7:p.Ile149=
ENST00000589115.6:c.447C>A	ENSP00000466872.3:p.Ile149=
ENST00000354171.12:c.447C>A	ENSP00000346103.7:p.Ile149=
ENST00000585480.1:c.180C>A	ENSP00000467900.1:p.Ile60=
ENST00000587648.5:c.327C>A	ENSP00000468349.1:p.Ile109=
ENST00000588919.5:c.366C>A	ENSP00000464989.3:p.Ile122=
ENST00000589115.5:c.447C>A	ENSP00000466872.2:p.Ile149=
ENST00000592940.2:n.386C>A
ENST00000593032.5:c.366C>A	ENSP00000465828.3:p.Ile122=
ENST00000611653.4:c.366C>A	ENSP00000483655.1:p.Ile122=
ENST00000616066.4:c.444C>A	ENSP00000485000.1:p.Ile148=
ENST00000622390.4:c.555C>A	ENSP00000477503.1:p.Ile185=
NM_001039847.2:c.447C>A	NP_001034936.1:p.Ile149=
NM_001039848.2:c.558C>A	NP_001034937.1:p.Ile186=
NM_002085.4:c.447C>A	NP_002076.2:p.Ile149=
NM_001039848.3:c.558C>A	NP_001034937.1:p.Ile186=
NM_001039847.3:c.447C>A	NP_001034936.1:p.Ile149=
NM_001039848.4:c.558C>A	NP_001034937.1:p.Ile186=
NM_001367832.1:c.366C>A	NP_001354761.1:p.Ile122=
NM_002085.5:c.447C>A MANE Select	NP_002076.2:p.Ile149=