Canonical Allele Identifier: CA402939117

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106245A>C (hg19) ; chr19:g.1106246A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106246A>C , CM000681.2:g.1106246A>C	GRCh38
NC_000019.9:g.1106245A>C , CM000681.1:g.1106245A>C	GRCh37
NC_000019.8:g.1057245A>C	NCBI36
NG_050621.1:g.7321A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.592A>C	ENSP00000473614.3:p.Ile198Leu
ENST00000593032.6:c.461A>C	ENSP00000465828.4:p.His154Pro
ENST00000706713.1:c.475A>C	ENSP00000516510.1:p.Ile159Leu
ENST00000706714.1:c.461A>C	ENSP00000516511.1:p.His154Pro
ENST00000706715.1:c.97A>C	ENSP00000516512.1:p.Ile33Leu
ENST00000354171.13:c.481A>C MANE Select	ENSP00000346103.7:p.Ile161Leu
ENST00000589115.6:c.477-154A>C	ENSP00000466872.3:n.477-154A>C
ENST00000354171.12:c.481A>C	ENSP00000346103.7:p.Ile161Leu
ENST00000585480.1:c.214A>C	ENSP00000467900.1:p.Ile72Leu
ENST00000587648.5:c.361A>C	ENSP00000468349.1:p.Ile121Leu
ENST00000588919.5:c.400A>C	ENSP00000464989.3:p.Ile134Leu
ENST00000589115.5:c.477-154A>C	ENSP00000466872.2:n.477-154A>C
ENST00000592940.2:n.852A>C
ENST00000593032.5:c.461A>C	ENSP00000465828.3:p.His154Pro
ENST00000611653.4:c.400A>C	ENSP00000483655.1:p.Ile134Leu
ENST00000616066.4:c.478A>C	ENSP00000485000.1:p.Ile160Leu
ENST00000622390.4:c.589A>C	ENSP00000477503.1:p.Ile197Leu
NM_001039847.2:c.481A>C	NP_001034936.1:p.Ile161Leu
NM_001039848.2:c.592A>C	NP_001034937.1:p.Ile198Leu
NM_002085.4:c.481A>C	NP_002076.2:p.Ile161Leu
NM_001039848.3:c.592A>C	NP_001034937.1:p.Ile198Leu
NM_001039847.3:c.481A>C	NP_001034936.1:p.Ile161Leu
NM_001039848.4:c.592A>C	NP_001034937.1:p.Ile198Leu
NM_001367832.1:c.400A>C	NP_001354761.1:p.Ile134Leu
NM_002085.5:c.481A>C MANE Select	NP_002076.2:p.Ile161Leu