Canonical Allele Identifier: CA402939667

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106403T>C (hg19) ; chr19:g.1106404T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106404T>C , CM000681.2:g.1106404T>C	GRCh38
NC_000019.9:g.1106403T>C , CM000681.1:g.1106403T>C	GRCh37
NC_000019.8:g.1057403T>C	NCBI36
NG_050621.1:g.7479T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.617T>C	ENSP00000473614.3:p.Leu206Pro
ENST00000593032.6:c.486T>C	ENSP00000465828.4:p.Pro162=
ENST00000706713.1:c.500T>C	ENSP00000516510.1:p.Leu167Pro
ENST00000706714.1:c.486T>C	ENSP00000516511.1:p.Pro162=
ENST00000706715.1:c.122T>C	ENSP00000516512.1:p.Leu41Pro
ENST00000354171.13:c.506T>C MANE Select	ENSP00000346103.7:p.Leu169Pro
ENST00000589115.6:c.481T>C	ENSP00000466872.3:p.Ser161Pro
ENST00000354171.12:c.506T>C	ENSP00000346103.7:p.Leu169Pro
ENST00000585480.1:c.239T>C	ENSP00000467900.1:p.Leu80Pro
ENST00000587648.5:c.386T>C	ENSP00000468349.1:p.Leu129Pro
ENST00000588919.5:c.447T>C	ENSP00000464989.3:p.Pro149=
ENST00000589115.5:c.481T>C	ENSP00000466872.2:p.Ser161Pro
ENST00000592940.2:n.877T>C
ENST00000593032.5:c.486T>C	ENSP00000465828.3:p.Pro162=
ENST00000611653.4:c.425T>C	ENSP00000483655.1:p.Leu142Pro
ENST00000616066.4:c.503T>C	ENSP00000485000.1:p.Leu168Pro
ENST00000622390.4:c.614T>C	ENSP00000477503.1:p.Leu205Pro
NM_001039847.2:c.528T>C	NP_001034936.1:p.Pro176=
NM_001039848.2:c.617T>C	NP_001034937.1:p.Leu206Pro
NM_002085.4:c.506T>C	NP_002076.2:p.Leu169Pro
NM_001039848.3:c.617T>C	NP_001034937.1:p.Leu206Pro
NM_001039847.3:c.528T>C	NP_001034936.1:p.Pro176=
NM_001039848.4:c.617T>C	NP_001034937.1:p.Leu206Pro
NM_001367832.1:c.425T>C	NP_001354761.1:p.Leu142Pro
NM_002085.5:c.506T>C MANE Select	NP_002076.2:p.Leu169Pro