Canonical Allele Identifier: CA402940626

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106672C>G (hg19) ; chr19:g.1106673C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106673C>G , CM000681.2:g.1106673C>G	GRCh38
NC_000019.9:g.1106672C>G , CM000681.1:g.1106672C>G	GRCh37
NC_000019.8:g.1057672C>G	NCBI36
NG_050621.1:g.7748C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*101C>G	ENSP00000473614.3:n.*101C>G
ENST00000593032.6:c.675C>G	ENSP00000465828.4:p.Asp225Glu
ENST00000706713.1:c.*101C>G	ENSP00000516510.1:n.*101C>G
ENST00000706714.1:c.675C>G	ENSP00000516511.1:p.Asp225Glu
ENST00000706715.1:c.*101C>G	ENSP00000516512.1:n.*101C>G
ENST00000354171.13:c.*101C>G MANE Select	ENSP00000346103.7:n.*101C>G
ENST00000589115.6:c.*127C>G	ENSP00000466872.3:n.*127C>G
ENST00000354171.12:c.*101C>G	ENSP00000346103.7:n.*101C>G
ENST00000585480.1:c.395C>G	ENSP00000467900.1:p.Thr132Ser
ENST00000588919.5:c.636C>G	ENSP00000464989.3:p.Asp212Glu
ENST00000589115.5:c.*127C>G	ENSP00000466872.2:n.*127C>G
ENST00000592940.2:n.1066C>G
ENST00000611653.4:c.*101C>G	ENSP00000483655.1:n.*101C>G
ENST00000616066.4:c.*101C>G	ENSP00000485000.1:n.*101C>G
ENST00000622390.4:c.*101C>G	ENSP00000477503.1:n.*101C>G
NM_001039847.2:c.*33C>G	NP_001034936.1:n.*33C>G
NM_001039848.2:c.*101C>G	NP_001034937.1:n.*101C>G
NM_002085.4:c.*101C>G	NP_002076.2:n.*101C>G
NM_001039848.3:c.*101C>G	NP_001034937.1:n.*101C>G
NM_001039847.3:c.*33C>G	NP_001034936.1:n.*33C>G
NM_001039848.4:c.*101C>G	NP_001034937.1:n.*101C>G
NM_001367832.1:c.*101C>G	NP_001354761.1:n.*101C>G
NM_002085.5:c.*101C>G MANE Select	NP_002076.2:n.*101C>G