Canonical Allele Identifier: CA402940726

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106725-C-G
• MyVariant Identifiers: chr19:g.1106724C>G (hg19) ; chr19:g.1106725C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106725C>G , CM000681.2:g.1106725C>G	GRCh38
NC_000019.9:g.1106724C>G , CM000681.1:g.1106724C>G	GRCh37
NC_000019.8:g.1057724C>G	NCBI36
NG_050621.1:g.7800C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*153C>G	ENSP00000473614.3:n.*153C>G
ENST00000593032.6:c.727C>G	ENSP00000465828.4:p.Leu243Val
ENST00000706713.1:c.*153C>G	ENSP00000516510.1:n.*153C>G
ENST00000706714.1:c.727C>G	ENSP00000516511.1:p.Leu243Val
ENST00000706715.1:c.*153C>G	ENSP00000516512.1:n.*153C>G
ENST00000354171.13:c.*153C>G MANE Select	ENSP00000346103.7:n.*153C>G
ENST00000589115.6:c.*179C>G	ENSP00000466872.3:n.*179C>G
ENST00000354171.12:c.*153C>G	ENSP00000346103.7:n.*153C>G
ENST00000585480.1:c.447C>G	ENSP00000467900.1:p.Gly149=
ENST00000588919.5:c.688C>G	ENSP00000464989.3:p.Leu230Val
ENST00000589115.5:c.*179C>G	ENSP00000466872.2:n.*179C>G
ENST00000592940.2:n.1118C>G
ENST00000611653.4:c.*153C>G	ENSP00000483655.1:n.*153C>G
ENST00000616066.4:c.*153C>G	ENSP00000485000.1:n.*153C>G
ENST00000622390.4:c.*153C>G	ENSP00000477503.1:n.*153C>G
NM_001039847.2:c.*85C>G	NP_001034936.1:n.*85C>G
NM_001039848.2:c.*153C>G	NP_001034937.1:n.*153C>G
NM_002085.4:c.*153C>G	NP_002076.2:n.*153C>G
NM_001039848.3:c.*153C>G	NP_001034937.1:n.*153C>G
NM_001039847.3:c.*85C>G	NP_001034936.1:n.*85C>G
NM_001039848.4:c.*153C>G	NP_001034937.1:n.*153C>G
NM_001367832.1:c.*153C>G	NP_001354761.1:n.*153C>G
NM_002085.5:c.*153C>G MANE Select	NP_002076.2:n.*153C>G