Canonical Allele Identifier: CA402937648

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105777A>G (hg19) ; chr19:g.1105778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105778A>G , CM000681.2:g.1105778A>G	GRCh38
NC_000019.9:g.1105777A>G , CM000681.1:g.1105777A>G	GRCh37
NC_000019.8:g.1056777A>G	NCBI36
NG_050621.1:g.6853A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.556A>G	ENSP00000473614.3:p.Ile186Val
ENST00000593032.6:c.364A>G	ENSP00000465828.4:p.Ile122Val
ENST00000706713.1:c.439A>G	ENSP00000516510.1:p.Ile147Val
ENST00000706714.1:c.364A>G	ENSP00000516511.1:p.Ile122Val
ENST00000706715.1:c.61A>G	ENSP00000516512.1:p.Ile21Val
ENST00000354171.13:c.445A>G MANE Select	ENSP00000346103.7:p.Ile149Val
ENST00000589115.6:c.445A>G	ENSP00000466872.3:p.Ile149Val
ENST00000354171.12:c.445A>G	ENSP00000346103.7:p.Ile149Val
ENST00000585480.1:c.178A>G	ENSP00000467900.1:p.Ile60Val
ENST00000587648.5:c.325A>G	ENSP00000468349.1:p.Ile109Val
ENST00000588919.5:c.364A>G	ENSP00000464989.3:p.Ile122Val
ENST00000589115.5:c.445A>G	ENSP00000466872.2:p.Ile149Val
ENST00000592940.2:n.384A>G
ENST00000593032.5:c.364A>G	ENSP00000465828.3:p.Ile122Val
ENST00000611653.4:c.364A>G	ENSP00000483655.1:p.Ile122Val
ENST00000616066.4:c.442A>G	ENSP00000485000.1:p.Ile148Val
ENST00000622390.4:c.553A>G	ENSP00000477503.1:p.Ile185Val
NM_001039847.2:c.445A>G	NP_001034936.1:p.Ile149Val
NM_001039848.2:c.556A>G	NP_001034937.1:p.Ile186Val
NM_002085.4:c.445A>G	NP_002076.2:p.Ile149Val
NM_001039848.3:c.556A>G	NP_001034937.1:p.Ile186Val
NM_001039847.3:c.445A>G	NP_001034936.1:p.Ile149Val
NM_001039848.4:c.556A>G	NP_001034937.1:p.Ile186Val
NM_001367832.1:c.364A>G	NP_001354761.1:p.Ile122Val
NM_002085.5:c.445A>G MANE Select	NP_002076.2:p.Ile149Val