Canonical Allele Identifier: CA402940614

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106666-G-T
• MyVariant Identifiers: chr19:g.1106665G>T (hg19) ; chr19:g.1106666G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106666G>T , CM000681.2:g.1106666G>T	GRCh38
NC_000019.9:g.1106665G>T , CM000681.1:g.1106665G>T	GRCh37
NC_000019.8:g.1057665G>T	NCBI36
NG_050621.1:g.7741G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*94G>T	ENSP00000473614.3:n.*94G>T
ENST00000593032.6:c.668G>T	ENSP00000465828.4:p.Gly223Val
ENST00000706713.1:c.*94G>T	ENSP00000516510.1:n.*94G>T
ENST00000706714.1:c.668G>T	ENSP00000516511.1:p.Gly223Val
ENST00000706715.1:c.*94G>T	ENSP00000516512.1:n.*94G>T
ENST00000354171.13:c.*94G>T MANE Select	ENSP00000346103.7:n.*94G>T
ENST00000589115.6:c.*120G>T	ENSP00000466872.3:n.*120G>T
ENST00000354171.12:c.*94G>T	ENSP00000346103.7:n.*94G>T
ENST00000585480.1:c.388G>T	ENSP00000467900.1:p.Gly130Trp
ENST00000588919.5:c.629G>T	ENSP00000464989.3:p.Gly210Val
ENST00000589115.5:c.*120G>T	ENSP00000466872.2:n.*120G>T
ENST00000592940.2:n.1059G>T
ENST00000611653.4:c.*94G>T	ENSP00000483655.1:n.*94G>T
ENST00000616066.4:c.*94G>T	ENSP00000485000.1:n.*94G>T
ENST00000622390.4:c.*94G>T	ENSP00000477503.1:n.*94G>T
NM_001039847.2:c.*26G>T	NP_001034936.1:n.*26G>T
NM_001039848.2:c.*94G>T	NP_001034937.1:n.*94G>T
NM_002085.4:c.*94G>T	NP_002076.2:n.*94G>T
NM_001039848.3:c.*94G>T	NP_001034937.1:n.*94G>T
NM_001039847.3:c.*26G>T	NP_001034936.1:n.*26G>T
NM_001039848.4:c.*94G>T	NP_001034937.1:n.*94G>T
NM_001367832.1:c.*94G>T	NP_001354761.1:n.*94G>T
NM_002085.5:c.*94G>T MANE Select	NP_002076.2:n.*94G>T