Canonical Allele Identifier: CA402940729

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106726-T-A
• MyVariant Identifiers: chr19:g.1106725T>A (hg19) ; chr19:g.1106726T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106726T>A , CM000681.2:g.1106726T>A	GRCh38
NC_000019.9:g.1106725T>A , CM000681.1:g.1106725T>A	GRCh37
NC_000019.8:g.1057725T>A	NCBI36
NG_050621.1:g.7801T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*154T>A	ENSP00000473614.3:n.*154T>A
ENST00000593032.6:c.728T>A	ENSP00000465828.4:p.Leu243His
ENST00000706713.1:c.*154T>A	ENSP00000516510.1:n.*154T>A
ENST00000706714.1:c.728T>A	ENSP00000516511.1:p.Leu243His
ENST00000706715.1:c.*154T>A	ENSP00000516512.1:n.*154T>A
ENST00000354171.13:c.*154T>A MANE Select	ENSP00000346103.7:n.*154T>A
ENST00000589115.6:c.*180T>A	ENSP00000466872.3:n.*180T>A
ENST00000354171.12:c.*154T>A	ENSP00000346103.7:n.*154T>A
ENST00000585480.1:c.448T>A	ENSP00000467900.1:p.Leu150Met
ENST00000588919.5:c.689T>A	ENSP00000464989.3:p.Leu230His
ENST00000589115.5:c.*180T>A	ENSP00000466872.2:n.*180T>A
ENST00000592940.2:n.1119T>A
ENST00000611653.4:c.*154T>A	ENSP00000483655.1:n.*154T>A
ENST00000616066.4:c.*154T>A	ENSP00000485000.1:n.*154T>A
ENST00000622390.4:c.*154T>A	ENSP00000477503.1:n.*154T>A
NM_001039847.2:c.*86T>A	NP_001034936.1:n.*86T>A
NM_001039848.2:c.*154T>A	NP_001034937.1:n.*154T>A
NM_002085.4:c.*154T>A	NP_002076.2:n.*154T>A
NM_001039848.3:c.*154T>A	NP_001034937.1:n.*154T>A
NM_001039847.3:c.*86T>A	NP_001034936.1:n.*86T>A
NM_001039848.4:c.*154T>A	NP_001034937.1:n.*154T>A
NM_001367832.1:c.*154T>A	NP_001354761.1:n.*154T>A
NM_002085.5:c.*154T>A MANE Select	NP_002076.2:n.*154T>A