Canonical Allele Identifier: CA402939133

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106248-C-T
• MyVariant Identifiers: chr19:g.1106247C>T (hg19) ; chr19:g.1106248C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106248C>T , CM000681.2:g.1106248C>T	GRCh38
NC_000019.9:g.1106247C>T , CM000681.1:g.1106247C>T	GRCh37
NC_000019.8:g.1057247C>T	NCBI36
NG_050621.1:g.7323C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.594C>T	ENSP00000473614.3:p.Ile198=
ENST00000593032.6:c.463C>T	ENSP00000465828.4:p.Gln155Ter
ENST00000706713.1:c.477C>T	ENSP00000516510.1:p.Ile159=
ENST00000706714.1:c.463C>T	ENSP00000516511.1:p.Gln155Ter
ENST00000706715.1:c.99C>T	ENSP00000516512.1:p.Ile33=
ENST00000354171.13:c.483C>T MANE Select	ENSP00000346103.7:p.Ile161=
ENST00000589115.6:c.477-152C>T	ENSP00000466872.3:n.477-152C>T
ENST00000354171.12:c.483C>T	ENSP00000346103.7:p.Ile161=
ENST00000585480.1:c.216C>T	ENSP00000467900.1:p.Ile72=
ENST00000587648.5:c.363C>T	ENSP00000468349.1:p.Ile121=
ENST00000588919.5:c.402C>T	ENSP00000464989.3:p.Ile134=
ENST00000589115.5:c.477-152C>T	ENSP00000466872.2:n.477-152C>T
ENST00000592940.2:n.854C>T
ENST00000593032.5:c.463C>T	ENSP00000465828.3:p.Gln155Ter
ENST00000611653.4:c.402C>T	ENSP00000483655.1:p.Ile134=
ENST00000616066.4:c.480C>T	ENSP00000485000.1:p.Ile160=
ENST00000622390.4:c.591C>T	ENSP00000477503.1:p.Ile197=
NM_001039847.2:c.483C>T	NP_001034936.1:p.Ile161=
NM_001039848.2:c.594C>T	NP_001034937.1:p.Ile198=
NM_002085.4:c.483C>T	NP_002076.2:p.Ile161=
NM_001039848.3:c.594C>T	NP_001034937.1:p.Ile198=
NM_001039847.3:c.483C>T	NP_001034936.1:p.Ile161=
NM_001039848.4:c.594C>T	NP_001034937.1:p.Ile198=
NM_001367832.1:c.402C>T	NP_001354761.1:p.Ile134=
NM_002085.5:c.483C>T MANE Select	NP_002076.2:p.Ile161=