Canonical Allele Identifier: CA402939098

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106242G>T (hg19) ; chr19:g.1106243G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106243G>T , CM000681.2:g.1106243G>T	GRCh38
NC_000019.9:g.1106242G>T , CM000681.1:g.1106242G>T	GRCh37
NC_000019.8:g.1057242G>T	NCBI36
NG_050621.1:g.7318G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.589G>T	ENSP00000473614.3:p.Ala197Ser
ENST00000593032.6:c.458G>T	ENSP00000465828.4:p.Cys153Phe
ENST00000706713.1:c.472G>T	ENSP00000516510.1:p.Ala158Ser
ENST00000706714.1:c.458G>T	ENSP00000516511.1:p.Cys153Phe
ENST00000706715.1:c.94G>T	ENSP00000516512.1:p.Ala32Ser
ENST00000354171.13:c.478G>T MANE Select	ENSP00000346103.7:p.Ala160Ser
ENST00000589115.6:c.477-157G>T	ENSP00000466872.3:n.477-157G>T
ENST00000354171.12:c.478G>T	ENSP00000346103.7:p.Ala160Ser
ENST00000585480.1:c.211G>T	ENSP00000467900.1:p.Ala71Ser
ENST00000587648.5:c.358G>T	ENSP00000468349.1:p.Ala120Ser
ENST00000588919.5:c.397G>T	ENSP00000464989.3:p.Ala133Ser
ENST00000589115.5:c.477-157G>T	ENSP00000466872.2:n.477-157G>T
ENST00000592940.2:n.849G>T
ENST00000593032.5:c.458G>T	ENSP00000465828.3:p.Cys153Phe
ENST00000611653.4:c.397G>T	ENSP00000483655.1:p.Ala133Ser
ENST00000616066.4:c.475G>T	ENSP00000485000.1:p.Ala159Ser
ENST00000622390.4:c.586G>T	ENSP00000477503.1:p.Ala196Ser
NM_001039847.2:c.478G>T	NP_001034936.1:p.Ala160Ser
NM_001039848.2:c.589G>T	NP_001034937.1:p.Ala197Ser
NM_002085.4:c.478G>T	NP_002076.2:p.Ala160Ser
NM_001039848.3:c.589G>T	NP_001034937.1:p.Ala197Ser
NM_001039847.3:c.478G>T	NP_001034936.1:p.Ala160Ser
NM_001039848.4:c.589G>T	NP_001034937.1:p.Ala197Ser
NM_001367832.1:c.397G>T	NP_001354761.1:p.Ala133Ser
NM_002085.5:c.478G>T MANE Select	NP_002076.2:p.Ala160Ser