Canonical Allele Identifier: CA2588207278

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105867-A-ACGCTCACGTCCATG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105867_1105868insCGCTCACGTCCATG , CM000681.2:g.1105867_1105868insCGCTCACGTCCATG	GRCh38
NC_000019.9:g.1105866_1105867insCGCTCACGTCCATG , CM000681.1:g.1105866_1105867insCGCTCACGTCCATG	GRCh37
NC_000019.8:g.1056866_1056867insCGCTCACGTCCATG	NCBI36
NG_050621.1:g.6942_6943insCGCTCACGTCCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+58_587+59insCGCTCACGTCCATG	ENSP00000473614.3:n.587+58_587+59insCGCTCACGTCCATG
ENST00000593032.6:c.395+58_395+59insCGCTCACGTCCATG	ENSP00000465828.4:n.395+58_395+59insCGCTCACGTCCATG
ENST00000706713.1:c.470+58_470+59insCGCTCACGTCCATG	ENSP00000516510.1:n.470+58_470+59insCGCTCACGTCCATG
ENST00000706714.1:c.395+58_395+59insCGCTCACGTCCATG	ENSP00000516511.1:n.395+58_395+59insCGCTCACGTCCATG
ENST00000706715.1:c.92+58_92+59insCGCTCACGTCCATG	ENSP00000516512.1:n.92+58_92+59insCGCTCACGTCCATG
ENST00000354171.13:c.476+58_476+59insCGCTCACGTCCATG MANE Select	ENSP00000346103.7:n.476+58_476+59insCGCTCACGTCCATG
ENST00000589115.6:c.476+58_476+59insCGCTCACGTCCATG	ENSP00000466872.3:n.476+58_476+59insCGCTCACGTCCATG
ENST00000354171.12:c.476+58_476+59insCGCTCACGTCCATG	ENSP00000346103.7:n.476+58_476+59insCGCTCACGTCCATG
ENST00000585480.1:c.209+58_209+59insCGCTCACGTCCATG	ENSP00000467900.1:n.209+58_209+59insCGCTCACGTCCATG
ENST00000587648.5:c.356+58_356+59insCGCTCACGTCCATG	ENSP00000468349.1:n.356+58_356+59insCGCTCACGTCCATG
ENST00000588919.5:c.395+58_395+59insCGCTCACGTCCATG	ENSP00000464989.3:n.395+58_395+59insCGCTCACGTCCATG
ENST00000589115.5:c.476+58_476+59insCGCTCACGTCCATG	ENSP00000466872.2:n.476+58_476+59insCGCTCACGTCCATG
ENST00000592940.2:n.473_474insCGCTCACGTCCATG
ENST00000593032.5:c.395+58_395+59insCGCTCACGTCCATG	ENSP00000465828.3:n.395+58_395+59insCGCTCACGTCCATG
ENST00000611653.4:c.395+58_395+59insCGCTCACGTCCATG	ENSP00000483655.1:n.395+58_395+59insCGCTCACGTCCATG
ENST00000616066.4:c.473+58_473+59insCGCTCACGTCCATG	ENSP00000485000.1:n.473+58_473+59insCGCTCACGTCCATG
ENST00000622390.4:c.584+58_584+59insCGCTCACGTCCATG	ENSP00000477503.1:n.584+58_584+59insCGCTCACGTCCATG
NM_001039847.2:c.476+58_476+59insCGCTCACGTCCATG	NP_001034936.1:n.476+58_476+59insCGCTCACGTCCATG
NM_001039848.2:c.587+58_587+59insCGCTCACGTCCATG	NP_001034937.1:n.587+58_587+59insCGCTCACGTCCATG
NM_002085.4:c.476+58_476+59insCGCTCACGTCCATG	NP_002076.2:n.476+58_476+59insCGCTCACGTCCATG
NM_001039848.3:c.587+58_587+59insCGCTCACGTCCATG	NP_001034937.1:n.587+58_587+59insCGCTCACGTCCATG
NM_001039847.3:c.476+58_476+59insCGCTCACGTCCATG	NP_001034936.1:n.476+58_476+59insCGCTCACGTCCATG
NM_001039848.4:c.587+58_587+59insCGCTCACGTCCATG	NP_001034937.1:n.587+58_587+59insCGCTCACGTCCATG
NM_001367832.1:c.395+58_395+59insCGCTCACGTCCATG	NP_001354761.1:n.395+58_395+59insCGCTCACGTCCATG
NM_002085.5:c.476+58_476+59insCGCTCACGTCCATG MANE Select	NP_002076.2:n.476+58_476+59insCGCTCACGTCCATG