Canonical Allele Identifier: CA402940543

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106632A>T (hg19) ; chr19:g.1106633A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106633A>T , CM000681.2:g.1106633A>T	GRCh38
NC_000019.9:g.1106632A>T , CM000681.1:g.1106632A>T	GRCh37
NC_000019.8:g.1057632A>T	NCBI36
NG_050621.1:g.7708A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*61A>T	ENSP00000473614.3:n.*61A>T
ENST00000593032.6:c.635A>T	ENSP00000465828.4:p.His212Leu
ENST00000706713.1:c.*61A>T	ENSP00000516510.1:n.*61A>T
ENST00000706714.1:c.635A>T	ENSP00000516511.1:p.His212Leu
ENST00000706715.1:c.*61A>T	ENSP00000516512.1:n.*61A>T
ENST00000354171.13:c.*61A>T MANE Select	ENSP00000346103.7:n.*61A>T
ENST00000589115.6:c.*87A>T	ENSP00000466872.3:n.*87A>T
ENST00000354171.12:c.*61A>T	ENSP00000346103.7:n.*61A>T
ENST00000585480.1:c.355A>T	ENSP00000467900.1:p.Thr119Ser
ENST00000588919.5:c.596A>T	ENSP00000464989.3:p.His199Leu
ENST00000589115.5:c.*87A>T	ENSP00000466872.2:n.*87A>T
ENST00000592940.2:n.1026A>T
ENST00000611653.4:c.*61A>T	ENSP00000483655.1:n.*61A>T
ENST00000616066.4:c.*61A>T	ENSP00000485000.1:n.*61A>T
ENST00000622390.4:c.*61A>T	ENSP00000477503.1:n.*61A>T
NM_001039847.2:c.677A>T	NP_001034936.1:p.His226Leu
NM_001039848.2:c.*61A>T	NP_001034937.1:n.*61A>T
NM_002085.4:c.*61A>T	NP_002076.2:n.*61A>T
NM_001039848.3:c.*61A>T	NP_001034937.1:n.*61A>T
NM_001039847.3:c.677A>T	NP_001034936.1:p.His226Leu
NM_001039848.4:c.*61A>T	NP_001034937.1:n.*61A>T
NM_001367832.1:c.*61A>T	NP_001354761.1:n.*61A>T
NM_002085.5:c.*61A>T MANE Select	NP_002076.2:n.*61A>T