Canonical Allele Identifier: CA402940034

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106436A>C (hg19) ; chr19:g.1106437A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106437A>C , CM000681.2:g.1106437A>C	GRCh38
NC_000019.9:g.1106436A>C , CM000681.1:g.1106436A>C	GRCh37
NC_000019.8:g.1057436A>C	NCBI36
NG_050621.1:g.7512A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.650A>C	ENSP00000473614.3:p.Tyr217Ser
ENST00000593032.6:c.519A>C	ENSP00000465828.4:p.Leu173=
ENST00000706713.1:c.533A>C	ENSP00000516510.1:p.Tyr178Ser
ENST00000706714.1:c.519A>C	ENSP00000516511.1:p.Leu173=
ENST00000706715.1:c.155A>C	ENSP00000516512.1:p.Tyr52Ser
ENST00000354171.13:c.539A>C MANE Select	ENSP00000346103.7:p.Tyr180Ser
ENST00000589115.6:c.514A>C	ENSP00000466872.3:p.Thr172Pro
ENST00000354171.12:c.539A>C	ENSP00000346103.7:p.Tyr180Ser
ENST00000585480.1:c.272A>C	ENSP00000467900.1:p.Tyr91Ser
ENST00000587648.5:c.419A>C	ENSP00000468349.1:p.Tyr140Ser
ENST00000588919.5:c.480A>C	ENSP00000464989.3:p.Leu160=
ENST00000589115.5:c.514A>C	ENSP00000466872.2:p.Thr172Pro
ENST00000592940.2:n.910A>C
ENST00000593032.5:c.519A>C	ENSP00000465828.3:p.Leu173=
ENST00000611653.4:c.458A>C	ENSP00000483655.1:p.Tyr153Ser
ENST00000616066.4:c.536A>C	ENSP00000485000.1:p.Tyr179Ser
ENST00000622390.4:c.647A>C	ENSP00000477503.1:p.Tyr216Ser
NM_001039847.2:c.561A>C	NP_001034936.1:p.Leu187=
NM_001039848.2:c.650A>C	NP_001034937.1:p.Tyr217Ser
NM_002085.4:c.539A>C	NP_002076.2:p.Tyr180Ser
NM_001039848.3:c.650A>C	NP_001034937.1:p.Tyr217Ser
NM_001039847.3:c.561A>C	NP_001034936.1:p.Leu187=
NM_001039848.4:c.650A>C	NP_001034937.1:p.Tyr217Ser
NM_001367832.1:c.458A>C	NP_001354761.1:p.Tyr153Ser
NM_002085.5:c.539A>C MANE Select	NP_002076.2:p.Tyr180Ser