Canonical Allele Identifier: CA2317520541

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106279_1106280delinsTG , CM000681.2:g.1106279_1106280delinsTG	GRCh38
NC_000019.9:g.1106278_1106279delinsTG , CM000681.1:g.1106278_1106279delinsTG	GRCh37
NC_000019.8:g.1057278_1057279delinsTG	NCBI36
NG_050621.1:g.7354_7355delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.612+13_612+14delinsTG	ENSP00000473614.3:n.612+13_612+14delinsTG
ENST00000593032.6:c.481+13_481+14delinsTG	ENSP00000465828.4:n.481+13_481+14delinsTG
ENST00000706713.1:c.495+13_495+14delinsTG	ENSP00000516510.1:n.495+13_495+14delinsTG
ENST00000706714.1:c.481+13_481+14delinsTG	ENSP00000516511.1:n.481+13_481+14delinsTG
ENST00000706715.1:c.117+13_117+14delinsTG	ENSP00000516512.1:n.117+13_117+14delinsTG
ENST00000354171.13:c.501+13_501+14delinsTG MANE Select	ENSP00000346103.7:n.501+13_501+14delinsTG
ENST00000589115.6:c.477-121_477-120delinsTG	ENSP00000466872.3:n.477-121_477-120delinsTG
ENST00000354171.12:c.501+13_501+14delinsTG	ENSP00000346103.7:n.501+13_501+14delinsTG
ENST00000585480.1:c.234+13_234+14delinsTG	ENSP00000467900.1:n.234+13_234+14delinsTG
ENST00000587648.5:c.381+13_381+14delinsTG	ENSP00000468349.1:n.381+13_381+14delinsTG
ENST00000588919.5:c.420+13_420+14delinsTG	ENSP00000464989.3:n.420+13_420+14delinsTG
ENST00000589115.5:c.477-121_477-120delinsTG	ENSP00000466872.2:n.477-121_477-120delinsTG
ENST00000592940.2:n.872+13_872+14delinsTG
ENST00000593032.5:c.481+13_481+14delinsTG	ENSP00000465828.3:n.481+13_481+14delinsTG
ENST00000611653.4:c.420+13_420+14delinsTG	ENSP00000483655.1:n.420+13_420+14delinsTG
ENST00000616066.4:c.498+13_498+14delinsTG	ENSP00000485000.1:n.498+13_498+14delinsTG
ENST00000622390.4:c.609+13_609+14delinsTG	ENSP00000477503.1:n.609+13_609+14delinsTG
NM_001039847.2:c.501+13_501+14delinsTG	NP_001034936.1:n.501+13_501+14delinsTG
NM_001039848.2:c.612+13_612+14delinsTG	NP_001034937.1:n.612+13_612+14delinsTG
NM_002085.4:c.501+13_501+14delinsTG	NP_002076.2:n.501+13_501+14delinsTG
NM_001039848.3:c.612+13_612+14delinsTG	NP_001034937.1:n.612+13_612+14delinsTG
NM_001039847.3:c.501+13_501+14delinsTG	NP_001034936.1:n.501+13_501+14delinsTG
NM_001039848.4:c.612+13_612+14delinsTG	NP_001034937.1:n.612+13_612+14delinsTG
NM_001367832.1:c.420+13_420+14delinsTG	NP_001354761.1:n.420+13_420+14delinsTG
NM_002085.5:c.501+13_501+14delinsTG MANE Select	NP_002076.2:n.501+13_501+14delinsTG