Canonical Allele Identifier: CA402940096

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106444A>C (hg19) ; chr19:g.1106445A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106445A>C , CM000681.2:g.1106445A>C	GRCh38
NC_000019.9:g.1106444A>C , CM000681.1:g.1106444A>C	GRCh37
NC_000019.8:g.1057444A>C	NCBI36
NG_050621.1:g.7520A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.658A>C	ENSP00000473614.3:p.Met220Leu
ENST00000593032.6:c.527A>C	ENSP00000465828.4:p.His176Pro
ENST00000706713.1:c.541A>C	ENSP00000516510.1:p.Met181Leu
ENST00000706714.1:c.527A>C	ENSP00000516511.1:p.His176Pro
ENST00000706715.1:c.163A>C	ENSP00000516512.1:p.Met55Leu
ENST00000354171.13:c.547A>C MANE Select	ENSP00000346103.7:p.Met183Leu
ENST00000589115.6:c.522A>C	ENSP00000466872.3:p.Pro174=
ENST00000354171.12:c.547A>C	ENSP00000346103.7:p.Met183Leu
ENST00000585480.1:c.280A>C	ENSP00000467900.1:p.Met94Leu
ENST00000587648.5:c.427A>C	ENSP00000468349.1:p.Met143Leu
ENST00000588919.5:c.488A>C	ENSP00000464989.3:p.His163Pro
ENST00000589115.5:c.522A>C	ENSP00000466872.2:p.Pro174=
ENST00000592940.2:n.918A>C
ENST00000611653.4:c.466A>C	ENSP00000483655.1:p.Met156Leu
ENST00000616066.4:c.544A>C	ENSP00000485000.1:p.Met182Leu
ENST00000622390.4:c.655A>C	ENSP00000477503.1:p.Met219Leu
NM_001039847.2:c.569A>C	NP_001034936.1:p.His190Pro
NM_001039848.2:c.658A>C	NP_001034937.1:p.Met220Leu
NM_002085.4:c.547A>C	NP_002076.2:p.Met183Leu
NM_001039848.3:c.658A>C	NP_001034937.1:p.Met220Leu
NM_001039847.3:c.569A>C	NP_001034936.1:p.His190Pro
NM_001039848.4:c.658A>C	NP_001034937.1:p.Met220Leu
NM_001367832.1:c.466A>C	NP_001354761.1:p.Met156Leu
NM_002085.5:c.547A>C MANE Select	NP_002076.2:p.Met183Leu