Canonical Allele Identifier: CA631298687

Gene: GPX4

Linked Data

• dbSNP Id: rs1568536779
• gnomAD v2: 19-1106303-TG-T
• gnomAD v4: 19-1106304-TG-T
• MyVariant Identifiers: chr19:g.1106304del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106306del , CM000681.2:g.1106306del	GRCh38
NC_000019.9:g.1106305del , CM000681.1:g.1106305del	GRCh37
NC_000019.8:g.1057305del	NCBI36
NG_050621.1:g.7381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.612+40del	ENSP00000473614.3:n.612+40del
ENST00000593032.6:c.481+40del	ENSP00000465828.4:n.481+40del
ENST00000706713.1:c.495+40del	ENSP00000516510.1:n.495+40del
ENST00000706714.1:c.481+40del	ENSP00000516511.1:n.481+40del
ENST00000706715.1:c.117+40del	ENSP00000516512.1:n.117+40del
ENST00000354171.13:c.501+40del MANE Select	ENSP00000346103.7:n.501+40del
ENST00000589115.6:c.477-94del	ENSP00000466872.3:n.477-94del
ENST00000354171.12:c.501+40del	ENSP00000346103.7:n.501+40del
ENST00000585480.1:c.234+40del	ENSP00000467900.1:n.234+40del
ENST00000587648.5:c.381+40del	ENSP00000468349.1:n.381+40del
ENST00000588919.5:c.420+40del	ENSP00000464989.3:n.420+40del
ENST00000589115.5:c.477-94del	ENSP00000466872.2:n.477-94del
ENST00000592940.2:n.872+40del
ENST00000593032.5:c.481+40del	ENSP00000465828.3:n.481+40del
ENST00000611653.4:c.420+40del	ENSP00000483655.1:n.420+40del
ENST00000616066.4:c.498+40del	ENSP00000485000.1:n.498+40del
ENST00000622390.4:c.609+40del	ENSP00000477503.1:n.609+40del
NM_001039847.2:c.501+40del	NP_001034936.1:n.501+40del
NM_001039848.2:c.612+40del	NP_001034937.1:n.612+40del
NM_002085.4:c.501+40del	NP_002076.2:n.501+40del
NM_001039848.3:c.612+40del	NP_001034937.1:n.612+40del
NM_001039847.3:c.501+40del	NP_001034936.1:n.501+40del
NM_001039848.4:c.612+40del	NP_001034937.1:n.612+40del
NM_001367832.1:c.420+40del	NP_001354761.1:n.420+40del
NM_002085.5:c.501+40del MANE Select	NP_002076.2:n.501+40del