Canonical Allele Identifier: CA402939266

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106264A>C (hg19) ; chr19:g.1106265A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106265A>C , CM000681.2:g.1106265A>C	GRCh38
NC_000019.9:g.1106264A>C , CM000681.1:g.1106264A>C	GRCh37
NC_000019.8:g.1057264A>C	NCBI36
NG_050621.1:g.7340A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.611A>C	ENSP00000473614.3:p.Lys204Thr
ENST00000593032.6:c.480A>C	ENSP00000465828.4:p.Gln160His
ENST00000706713.1:c.494A>C	ENSP00000516510.1:p.Lys165Thr
ENST00000706714.1:c.480A>C	ENSP00000516511.1:p.Gln160His
ENST00000706715.1:c.116A>C	ENSP00000516512.1:p.Lys39Thr
ENST00000354171.13:c.500A>C MANE Select	ENSP00000346103.7:p.Lys167Thr
ENST00000589115.6:c.477-135A>C	ENSP00000466872.3:n.477-135A>C
ENST00000354171.12:c.500A>C	ENSP00000346103.7:p.Lys167Thr
ENST00000585480.1:c.233A>C	ENSP00000467900.1:p.Lys78Thr
ENST00000587648.5:c.380A>C	ENSP00000468349.1:p.Lys127Thr
ENST00000588919.5:c.419A>C	ENSP00000464989.3:p.Lys140Thr
ENST00000589115.5:c.477-135A>C	ENSP00000466872.2:n.477-135A>C
ENST00000592940.2:n.871A>C
ENST00000593032.5:c.480A>C	ENSP00000465828.3:p.Gln160His
ENST00000611653.4:c.419A>C	ENSP00000483655.1:p.Lys140Thr
ENST00000616066.4:c.497A>C	ENSP00000485000.1:p.Lys166Thr
ENST00000622390.4:c.608A>C	ENSP00000477503.1:p.Lys203Thr
NM_001039847.2:c.500A>C	NP_001034936.1:p.Lys167Thr
NM_001039848.2:c.611A>C	NP_001034937.1:p.Lys204Thr
NM_002085.4:c.500A>C	NP_002076.2:p.Lys167Thr
NM_001039848.3:c.611A>C	NP_001034937.1:p.Lys204Thr
NM_001039847.3:c.500A>C	NP_001034936.1:p.Lys167Thr
NM_001039848.4:c.611A>C	NP_001034937.1:p.Lys204Thr
NM_001367832.1:c.419A>C	NP_001354761.1:p.Lys140Thr
NM_002085.5:c.500A>C MANE Select	NP_002076.2:p.Lys167Thr