Canonical Allele Identifier: CA504890875

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105662A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105663A>C , CM000681.2:g.1105663A>C	GRCh38
NC_000019.9:g.1105662A>C , CM000681.1:g.1105662A>C	GRCh37
NC_000019.8:g.1056662A>C	NCBI36
NG_050621.1:g.6738A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.441A>C	ENSP00000473614.3:p.Pro147=
ENST00000593032.6:c.249A>C	ENSP00000465828.4:p.Pro83=
ENST00000706713.1:c.324A>C	ENSP00000516510.1:p.Pro108=
ENST00000706714.1:c.249A>C	ENSP00000516511.1:p.Pro83=
ENST00000706715.1:c.-55A>C	ENSP00000516512.1:n.-55A>C
ENST00000354171.13:c.330A>C MANE Select	ENSP00000346103.7:p.Pro110=
ENST00000589115.6:c.330A>C	ENSP00000466872.3:p.Pro110=
ENST00000354171.12:c.330A>C	ENSP00000346103.7:p.Pro110=
ENST00000585362.6:c.441A>C	ENSP00000473614.2:p.Pro147=
ENST00000585480.1:c.63A>C	ENSP00000467900.1:p.Pro21=
ENST00000587648.5:c.210A>C	ENSP00000468349.1:p.Pro70=
ENST00000587932.2:n.264A>C
ENST00000588919.5:c.249A>C	ENSP00000464989.3:p.Pro83=
ENST00000589115.5:c.330A>C	ENSP00000466872.2:p.Pro110=
ENST00000592940.2:n.271-2A>C
ENST00000593032.5:c.249A>C	ENSP00000465828.3:p.Pro83=
ENST00000611653.4:c.249A>C	ENSP00000483655.1:p.Pro83=
ENST00000616066.4:c.327A>C	ENSP00000485000.1:p.Pro109=
ENST00000622390.4:c.438A>C	ENSP00000477503.1:p.Pro146=
NM_001039847.2:c.330A>C	NP_001034936.1:p.Pro110=
NM_001039848.2:c.441A>C	NP_001034937.1:p.Pro147=
NM_002085.4:c.330A>C	NP_002076.2:p.Pro110=
NM_001039848.3:c.441A>C	NP_001034937.1:p.Pro147=
NM_001039847.3:c.330A>C	NP_001034936.1:p.Pro110=
NM_001039848.4:c.441A>C	NP_001034937.1:p.Pro147=
NM_001367832.1:c.249A>C	NP_001354761.1:p.Pro83=
NM_002085.5:c.330A>C MANE Select	NP_002076.2:p.Pro110=