Canonical Allele Identifier: CA2588207816

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106318-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106318_1106319insTC , CM000681.2:g.1106318_1106319insTC	GRCh38
NC_000019.9:g.1106317_1106318insTC , CM000681.1:g.1106317_1106318insTC	GRCh37
NC_000019.8:g.1057317_1057318insTC	NCBI36
NG_050621.1:g.7393_7394insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.612+52_612+53insTC	ENSP00000473614.3:n.612+52_612+53insTC
ENST00000593032.6:c.481+52_481+53insTC	ENSP00000465828.4:n.481+52_481+53insTC
ENST00000706713.1:c.495+52_495+53insTC	ENSP00000516510.1:n.495+52_495+53insTC
ENST00000706714.1:c.481+52_481+53insTC	ENSP00000516511.1:n.481+52_481+53insTC
ENST00000706715.1:c.117+52_117+53insTC	ENSP00000516512.1:n.117+52_117+53insTC
ENST00000354171.13:c.501+52_501+53insTC MANE Select	ENSP00000346103.7:n.501+52_501+53insTC
ENST00000589115.6:c.477-82_477-81insTC	ENSP00000466872.3:n.477-82_477-81insTC
ENST00000354171.12:c.501+52_501+53insTC	ENSP00000346103.7:n.501+52_501+53insTC
ENST00000585480.1:c.234+52_234+53insTC	ENSP00000467900.1:n.234+52_234+53insTC
ENST00000587648.5:c.381+52_381+53insTC	ENSP00000468349.1:n.381+52_381+53insTC
ENST00000588919.5:c.420+52_420+53insTC	ENSP00000464989.3:n.420+52_420+53insTC
ENST00000589115.5:c.477-82_477-81insTC	ENSP00000466872.2:n.477-82_477-81insTC
ENST00000592940.2:n.872+52_872+53insTC
ENST00000593032.5:c.481+52_481+53insTC	ENSP00000465828.3:n.481+52_481+53insTC
ENST00000611653.4:c.420+52_420+53insTC	ENSP00000483655.1:n.420+52_420+53insTC
ENST00000616066.4:c.498+52_498+53insTC	ENSP00000485000.1:n.498+52_498+53insTC
ENST00000622390.4:c.609+52_609+53insTC	ENSP00000477503.1:n.609+52_609+53insTC
NM_001039847.2:c.501+52_501+53insTC	NP_001034936.1:n.501+52_501+53insTC
NM_001039848.2:c.612+52_612+53insTC	NP_001034937.1:n.612+52_612+53insTC
NM_002085.4:c.501+52_501+53insTC	NP_002076.2:n.501+52_501+53insTC
NM_001039848.3:c.612+52_612+53insTC	NP_001034937.1:n.612+52_612+53insTC
NM_001039847.3:c.501+52_501+53insTC	NP_001034936.1:n.501+52_501+53insTC
NM_001039848.4:c.612+52_612+53insTC	NP_001034937.1:n.612+52_612+53insTC
NM_001367832.1:c.420+52_420+53insTC	NP_001354761.1:n.420+52_420+53insTC
NM_002085.5:c.501+52_501+53insTC MANE Select	NP_002076.2:n.501+52_501+53insTC