Canonical Allele Identifier: CA9037556

Gene: GPX4

Linked Data

• dbSNP Id: rs775322412
• ExAC: 19:1106619 G / A
• gnomAD v2: 19-1106619-G-A
• gnomAD v4: 19-1106620-G-A
• MyVariant Identifiers: chr19:g.1106619G>A (hg19) ; chr19:g.1106620G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106620G>A , CM000681.2:g.1106620G>A	GRCh38
NC_000019.9:g.1106619G>A , CM000681.1:g.1106619G>A	GRCh37
NC_000019.8:g.1057619G>A	NCBI36
NG_050621.1:g.7695G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.*48G>A	ENSP00000473614.3:n.*48G>A
ENST00000593032.6:c.622G>A	ENSP00000465828.4:p.Ala208Thr
ENST00000706713.1:c.*48G>A	ENSP00000516510.1:n.*48G>A
ENST00000706714.1:c.622G>A	ENSP00000516511.1:p.Ala208Thr
ENST00000706715.1:c.*48G>A	ENSP00000516512.1:n.*48G>A
ENST00000354171.13:c.*48G>A MANE Select	ENSP00000346103.7:n.*48G>A
ENST00000589115.6:c.*74G>A	ENSP00000466872.3:n.*74G>A
ENST00000354171.12:c.*48G>A	ENSP00000346103.7:n.*48G>A
ENST00000585480.1:c.342G>A	ENSP00000467900.1:p.Glu114=
ENST00000588919.5:c.583G>A	ENSP00000464989.3:p.Ala195Thr
ENST00000589115.5:c.*74G>A	ENSP00000466872.2:n.*74G>A
ENST00000592940.2:n.1013G>A
ENST00000611653.4:c.*48G>A	ENSP00000483655.1:n.*48G>A
ENST00000616066.4:c.*48G>A	ENSP00000485000.1:n.*48G>A
ENST00000622390.4:c.*48G>A	ENSP00000477503.1:n.*48G>A
NM_001039847.2:c.664G>A	NP_001034936.1:p.Ala222Thr
NM_001039848.2:c.*48G>A	NP_001034937.1:n.*48G>A
NM_002085.4:c.*48G>A	NP_002076.2:n.*48G>A
NM_001039848.3:c.*48G>A	NP_001034937.1:n.*48G>A
NM_001039847.3:c.664G>A	NP_001034936.1:p.Ala222Thr
NM_001039848.4:c.*48G>A	NP_001034937.1:n.*48G>A
NM_001367832.1:c.*48G>A	NP_001354761.1:n.*48G>A
NM_002085.5:c.*48G>A MANE Select	NP_002076.2:n.*48G>A