Canonical Allele Identifier: CA992488304

Gene: GPX4

Linked Data

• gnomAD v3: 19-1106031-GGACAGGATGGCTCGGGGGCCTGTGGGGGGCTGTTGGGACTCTCACACTGCATGGCCTCCTGGGGTAAGATGGCTCTGGGGGGGCTTGGGGGCACTGTGGCTGTGGAGGCAGCCGGGGAAGCTCACACCCTTGTGGCCTCCTGGA-G
• gnomAD v4: 19-1106031-GGACAGGATGGCTCGGGGGCCTGTGGGGGGCTGTTGGGACTCTCACACTGCATGGCCTCCTGGGGTAAGATGGCTCTGGGGGGGCTTGGGGGCACTGTGGCTGTGGAGGCAGCCGGGGAAGCTCACACCCTTGTGGCCTCCTGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106039_1106182del , CM000681.2:g.1106039_1106182del	GRCh38
NC_000019.9:g.1106038_1106181del , CM000681.1:g.1106038_1106181del	GRCh37
NC_000019.8:g.1057038_1057181del	NCBI36
NG_050621.1:g.7114_7257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-203_588-60del	ENSP00000473614.3:n.588-203_588-60del
ENST00000593032.6:c.396-142_397del
ENST00000706713.1:c.471-203_471-60del	ENSP00000516510.1:n.471-203_471-60del
ENST00000706714.1:c.396-142_397del
ENST00000706715.1:c.93-203_93-60del	ENSP00000516512.1:n.93-203_93-60del
ENST00000354171.13:c.477-203_477-60del MANE Select	ENSP00000346103.7:n.477-203_477-60del
ENST00000589115.6:c.476+230_477-218del	ENSP00000466872.3:n.476+230_477-218del
ENST00000354171.12:c.477-203_477-60del	ENSP00000346103.7:n.477-203_477-60del
ENST00000585480.1:c.210-203_210-60del	ENSP00000467900.1:n.210-203_210-60del
ENST00000587648.5:c.357-203_357-60del	ENSP00000468349.1:n.357-203_357-60del
ENST00000588919.5:c.396-203_396-60del	ENSP00000464989.3:n.396-203_396-60del
ENST00000589115.5:c.476+230_477-218del	ENSP00000466872.2:n.476+230_477-218del
ENST00000592940.2:n.645_788del
ENST00000593032.5:c.396-142_397del
ENST00000611653.4:c.396-203_396-60del	ENSP00000483655.1:n.396-203_396-60del
ENST00000616066.4:c.474-203_474-60del	ENSP00000485000.1:n.474-203_474-60del
ENST00000622390.4:c.585-203_585-60del	ENSP00000477503.1:n.585-203_585-60del
NM_001039847.2:c.477-203_477-60del	NP_001034936.1:n.477-203_477-60del
NM_001039848.2:c.588-203_588-60del	NP_001034937.1:n.588-203_588-60del
NM_002085.4:c.477-203_477-60del	NP_002076.2:n.477-203_477-60del
NM_001039848.3:c.588-203_588-60del	NP_001034937.1:n.588-203_588-60del
NM_001039847.3:c.477-203_477-60del	NP_001034936.1:n.477-203_477-60del
NM_001039848.4:c.588-203_588-60del	NP_001034937.1:n.588-203_588-60del
NM_001367832.1:c.396-203_396-60del	NP_001354761.1:n.396-203_396-60del
NM_002085.5:c.477-203_477-60del MANE Select	NP_002076.2:n.477-203_477-60del