Canonical Allele Identifier: CA2588207797

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106277-TGTGGGGGGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106279_1106288del , CM000681.2:g.1106279_1106288del	GRCh38
NC_000019.9:g.1106278_1106287del , CM000681.1:g.1106278_1106287del	GRCh37
NC_000019.8:g.1057278_1057287del	NCBI36
NG_050621.1:g.7354_7363del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.612+13_612+22del	ENSP00000473614.3:n.612+13_612+22del
ENST00000593032.6:c.481+13_481+22del	ENSP00000465828.4:n.481+13_481+22del
ENST00000706713.1:c.495+13_495+22del	ENSP00000516510.1:n.495+13_495+22del
ENST00000706714.1:c.481+13_481+22del	ENSP00000516511.1:n.481+13_481+22del
ENST00000706715.1:c.117+13_117+22del	ENSP00000516512.1:n.117+13_117+22del
ENST00000354171.13:c.501+13_501+22del MANE Select	ENSP00000346103.7:n.501+13_501+22del
ENST00000589115.6:c.477-121_477-112del	ENSP00000466872.3:n.477-121_477-112del
ENST00000354171.12:c.501+13_501+22del	ENSP00000346103.7:n.501+13_501+22del
ENST00000585480.1:c.234+13_234+22del	ENSP00000467900.1:n.234+13_234+22del
ENST00000587648.5:c.381+13_381+22del	ENSP00000468349.1:n.381+13_381+22del
ENST00000588919.5:c.420+13_420+22del	ENSP00000464989.3:n.420+13_420+22del
ENST00000589115.5:c.477-121_477-112del	ENSP00000466872.2:n.477-121_477-112del
ENST00000592940.2:n.872+13_872+22del
ENST00000593032.5:c.481+13_481+22del	ENSP00000465828.3:n.481+13_481+22del
ENST00000611653.4:c.420+13_420+22del	ENSP00000483655.1:n.420+13_420+22del
ENST00000616066.4:c.498+13_498+22del	ENSP00000485000.1:n.498+13_498+22del
ENST00000622390.4:c.609+13_609+22del	ENSP00000477503.1:n.609+13_609+22del
NM_001039847.2:c.501+13_501+22del	NP_001034936.1:n.501+13_501+22del
NM_001039848.2:c.612+13_612+22del	NP_001034937.1:n.612+13_612+22del
NM_002085.4:c.501+13_501+22del	NP_002076.2:n.501+13_501+22del
NM_001039848.3:c.612+13_612+22del	NP_001034937.1:n.612+13_612+22del
NM_001039847.3:c.501+13_501+22del	NP_001034936.1:n.501+13_501+22del
NM_001039848.4:c.612+13_612+22del	NP_001034937.1:n.612+13_612+22del
NM_001367832.1:c.420+13_420+22del	NP_001354761.1:n.420+13_420+22del
NM_002085.5:c.501+13_501+22del MANE Select	NP_002076.2:n.501+13_501+22del