Canonical Allele Identifier: CA402939159

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106251-G-C
• MyVariant Identifiers: chr19:g.1106250G>C (hg19) ; chr19:g.1106251G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106251G>C , CM000681.2:g.1106251G>C	GRCh38
NC_000019.9:g.1106250G>C , CM000681.1:g.1106250G>C	GRCh37
NC_000019.8:g.1057250G>C	NCBI36
NG_050621.1:g.7326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.597G>C	ENSP00000473614.3:p.Lys199Asn
ENST00000593032.6:c.466G>C	ENSP00000465828.4:p.Val156Leu
ENST00000706713.1:c.480G>C	ENSP00000516510.1:p.Lys160Asn
ENST00000706714.1:c.466G>C	ENSP00000516511.1:p.Val156Leu
ENST00000706715.1:c.102G>C	ENSP00000516512.1:p.Lys34Asn
ENST00000354171.13:c.486G>C MANE Select	ENSP00000346103.7:p.Lys162Asn
ENST00000589115.6:c.477-149G>C	ENSP00000466872.3:n.477-149G>C
ENST00000354171.12:c.486G>C	ENSP00000346103.7:p.Lys162Asn
ENST00000585480.1:c.219G>C	ENSP00000467900.1:p.Lys73Asn
ENST00000587648.5:c.366G>C	ENSP00000468349.1:p.Lys122Asn
ENST00000588919.5:c.405G>C	ENSP00000464989.3:p.Lys135Asn
ENST00000589115.5:c.477-149G>C	ENSP00000466872.2:n.477-149G>C
ENST00000592940.2:n.857G>C
ENST00000593032.5:c.466G>C	ENSP00000465828.3:p.Val156Leu
ENST00000611653.4:c.405G>C	ENSP00000483655.1:p.Lys135Asn
ENST00000616066.4:c.483G>C	ENSP00000485000.1:p.Lys161Asn
ENST00000622390.4:c.594G>C	ENSP00000477503.1:p.Lys198Asn
NM_001039847.2:c.486G>C	NP_001034936.1:p.Lys162Asn
NM_001039848.2:c.597G>C	NP_001034937.1:p.Lys199Asn
NM_002085.4:c.486G>C	NP_002076.2:p.Lys162Asn
NM_001039848.3:c.597G>C	NP_001034937.1:p.Lys199Asn
NM_001039847.3:c.486G>C	NP_001034936.1:p.Lys162Asn
NM_001039848.4:c.597G>C	NP_001034937.1:p.Lys199Asn
NM_001367832.1:c.405G>C	NP_001354761.1:p.Lys135Asn
NM_002085.5:c.486G>C MANE Select	NP_002076.2:p.Lys162Asn