Canonical Allele Identifier: CA504693866

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1104066C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104067C>G , CM000681.2:g.1104067C>G	GRCh38
NC_000019.9:g.1104066C>G , CM000681.1:g.1104066C>G	GRCh37
NC_000019.8:g.1055066C>G	NCBI36
NG_050621.1:g.5142C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593032.6:c.-58C>G	ENSP00000465828.4:n.-58C>G
ENST00000706713.1:c.24C>G	ENSP00000516510.1:p.Arg8=
ENST00000706714.1:c.-58C>G	ENSP00000516511.1:n.-58C>G
ENST00000354171.13:c.24C>G MANE Select	ENSP00000346103.7:p.Arg8=
ENST00000589115.6:c.24C>G	ENSP00000466872.3:p.Arg8=
ENST00000354171.12:c.24C>G	ENSP00000346103.7:p.Arg8=
ENST00000589115.5:c.24C>G	ENSP00000466872.2:p.Arg8=
ENST00000593032.5:c.-58C>G	ENSP00000465828.3:n.-58C>G
ENST00000611653.4:c.-58C>G	ENSP00000483655.1:n.-58C>G
ENST00000616066.4:c.24C>G	ENSP00000485000.1:p.Arg8=
NM_001039847.2:c.24C>G	NP_001034936.1:p.Arg8=
NM_002085.4:c.24C>G	NP_002076.2:p.Arg8=
NM_001039847.3:c.24C>G	NP_001034936.1:p.Arg8=
NM_001367832.1:c.-58C>G	NP_001354761.1:n.-58C>G
NM_002085.5:c.24C>G MANE Select	NP_002076.2:p.Arg8=