Canonical Allele Identifier: CA402940782

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106755T>A (hg19) ; chr19:g.1106756T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106756T>A , CM000681.2:g.1106756T>A	GRCh38
NC_000019.9:g.1106755T>A , CM000681.1:g.1106755T>A	GRCh37
NC_000019.8:g.1057755T>A	NCBI36
NG_050621.1:g.7831T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*184T>A	ENSP00000473614.3:n.*184T>A
ENST00000593032.6:c.758T>A	ENSP00000465828.4:p.Leu253Ter
ENST00000706713.1:c.*184T>A	ENSP00000516510.1:n.*184T>A
ENST00000706714.1:c.758T>A	ENSP00000516511.1:p.Leu253Ter
ENST00000706715.1:c.*184T>A	ENSP00000516512.1:n.*184T>A
ENST00000354171.13:c.*184T>A MANE Select	ENSP00000346103.7:n.*184T>A
ENST00000589115.6:c.*210T>A	ENSP00000466872.3:n.*210T>A
ENST00000354171.12:c.*184T>A	ENSP00000346103.7:n.*184T>A
ENST00000585480.1:c.478T>A	ENSP00000467900.1:p.Cys160Ser
ENST00000588919.5:c.719T>A	ENSP00000464989.3:p.Leu240Ter
ENST00000589115.5:c.*210T>A	ENSP00000466872.2:n.*210T>A
ENST00000592940.2:n.1149T>A
ENST00000611653.4:c.*184T>A	ENSP00000483655.1:n.*184T>A
ENST00000616066.4:c.*184T>A	ENSP00000485000.1:n.*184T>A
ENST00000622390.4:c.*184T>A	ENSP00000477503.1:n.*184T>A
NM_001039847.2:c.*116T>A	NP_001034936.1:n.*116T>A
NM_001039848.2:c.*184T>A	NP_001034937.1:n.*184T>A
NM_002085.4:c.*184T>A	NP_002076.2:n.*184T>A
NM_001039848.3:c.*184T>A	NP_001034937.1:n.*184T>A
NM_001039847.3:c.*116T>A	NP_001034936.1:n.*116T>A
NM_001039848.4:c.*184T>A	NP_001034937.1:n.*184T>A
NM_001367832.1:c.*184T>A	NP_001354761.1:n.*184T>A
NM_002085.5:c.*184T>A MANE Select	NP_002076.2:n.*184T>A