Canonical Allele Identifier: CA402940531

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106626A>T (hg19) ; chr19:g.1106627A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106627A>T , CM000681.2:g.1106627A>T	GRCh38
NC_000019.9:g.1106626A>T , CM000681.1:g.1106626A>T	GRCh37
NC_000019.8:g.1057626A>T	NCBI36
NG_050621.1:g.7702A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.*55A>T	ENSP00000473614.3:n.*55A>T
ENST00000593032.6:c.629A>T	ENSP00000465828.4:p.His210Leu
ENST00000706713.1:c.*55A>T	ENSP00000516510.1:n.*55A>T
ENST00000706714.1:c.629A>T	ENSP00000516511.1:p.His210Leu
ENST00000706715.1:c.*55A>T	ENSP00000516512.1:n.*55A>T
ENST00000354171.13:c.*55A>T MANE Select	ENSP00000346103.7:n.*55A>T
ENST00000589115.6:c.*81A>T	ENSP00000466872.3:n.*81A>T
ENST00000354171.12:c.*55A>T	ENSP00000346103.7:n.*55A>T
ENST00000585480.1:c.349A>T	ENSP00000467900.1:p.Thr117Ser
ENST00000588919.5:c.590A>T	ENSP00000464989.3:p.His197Leu
ENST00000589115.5:c.*81A>T	ENSP00000466872.2:n.*81A>T
ENST00000592940.2:n.1020A>T
ENST00000611653.4:c.*55A>T	ENSP00000483655.1:n.*55A>T
ENST00000616066.4:c.*55A>T	ENSP00000485000.1:n.*55A>T
ENST00000622390.4:c.*55A>T	ENSP00000477503.1:n.*55A>T
NM_001039847.2:c.671A>T	NP_001034936.1:p.His224Leu
NM_001039848.2:c.*55A>T	NP_001034937.1:n.*55A>T
NM_002085.4:c.*55A>T	NP_002076.2:n.*55A>T
NM_001039848.3:c.*55A>T	NP_001034937.1:n.*55A>T
NM_001039847.3:c.671A>T	NP_001034936.1:p.His224Leu
NM_001039848.4:c.*55A>T	NP_001034937.1:n.*55A>T
NM_001367832.1:c.*55A>T	NP_001354761.1:n.*55A>T
NM_002085.5:c.*55A>T MANE Select	NP_002076.2:n.*55A>T