Canonical Allele Identifier: CA631298683

Gene: GPX4

Linked Data

• dbSNP Id: rs1568537692
• gnomAD v2: 19-1106496-G-GTA
• MyVariant Identifiers: chr19:g.1106496_1106497insTA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106497_1106498insTA , CM000681.2:g.1106497_1106498insTA	GRCh38
NC_000019.9:g.1106496_1106497insTA , CM000681.1:g.1106496_1106497insTA	GRCh37
NC_000019.8:g.1057496_1057497insTA	NCBI36
NG_050621.1:g.7572_7573insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.672+38_672+39insTA	ENSP00000473614.3:n.672+38_672+39insTA
ENST00000593032.6:c.541+38_541+39insTA	ENSP00000465828.4:n.541+38_541+39insTA
ENST00000706713.1:c.555+38_555+39insTA	ENSP00000516510.1:n.555+38_555+39insTA
ENST00000706714.1:c.541+38_541+39insTA	ENSP00000516511.1:n.541+38_541+39insTA
ENST00000706715.1:c.177+38_177+39insTA	ENSP00000516512.1:n.177+38_177+39insTA
ENST00000354171.13:c.561+38_561+39insTA MANE Select	ENSP00000346103.7:n.561+38_561+39insTA
ENST00000589115.6:c.536+38_536+39insTA	ENSP00000466872.3:n.536+38_536+39insTA
ENST00000354171.12:c.561+38_561+39insTA	ENSP00000346103.7:n.561+38_561+39insTA
ENST00000585480.1:c.294+38_294+39insTA	ENSP00000467900.1:n.294+38_294+39insTA
ENST00000587648.5:c.441+38_441+39insTA	ENSP00000468349.1:n.441+38_441+39insTA
ENST00000588919.5:c.502+38_502+39insTA	ENSP00000464989.3:n.502+38_502+39insTA
ENST00000589115.5:c.536+38_536+39insTA	ENSP00000466872.2:n.536+38_536+39insTA
ENST00000592940.2:n.932+38_932+39insTA
ENST00000611653.4:c.480+38_480+39insTA	ENSP00000483655.1:n.480+38_480+39insTA
ENST00000616066.4:c.558+38_558+39insTA	ENSP00000485000.1:n.558+38_558+39insTA
ENST00000622390.4:c.669+38_669+39insTA	ENSP00000477503.1:n.669+38_669+39insTA
NM_001039847.2:c.583+38_583+39insTA	NP_001034936.1:n.583+38_583+39insTA
NM_001039848.2:c.672+38_672+39insTA	NP_001034937.1:n.672+38_672+39insTA
NM_002085.4:c.561+38_561+39insTA	NP_002076.2:n.561+38_561+39insTA
NM_001039848.3:c.672+38_672+39insTA	NP_001034937.1:n.672+38_672+39insTA
NM_001039847.3:c.583+38_583+39insTA	NP_001034936.1:n.583+38_583+39insTA
NM_001039848.4:c.672+38_672+39insTA	NP_001034937.1:n.672+38_672+39insTA
NM_001367832.1:c.480+38_480+39insTA	NP_001354761.1:n.480+38_480+39insTA
NM_002085.5:c.561+38_561+39insTA MANE Select	NP_002076.2:n.561+38_561+39insTA