Canonical Allele Identifier: CA303992662

Gene: GPX4

Linked Data

• dbSNP Id: rs925722714
• gnomAD v2: 19-1104124-A-G
• gnomAD v4: 19-1104125-A-G
• MyVariant Identifiers: chr19:g.1104124A>G (hg19) ; chr19:g.1104125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104125A>G , CM000681.2:g.1104125A>G	GRCh38
NC_000019.9:g.1104124A>G , CM000681.1:g.1104124A>G	GRCh37
NC_000019.8:g.1055124A>G	NCBI36
NG_050621.1:g.5200A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593032.6:c.1A>G	ENSP00000465828.4:p.Met1Val
ENST00000706713.1:c.82A>G	ENSP00000516510.1:p.Met28Val
ENST00000706714.1:c.1A>G	ENSP00000516511.1:p.Met1Val
ENST00000354171.13:c.82A>G MANE Select	ENSP00000346103.7:p.Met28Val
ENST00000589115.6:c.82A>G	ENSP00000466872.3:p.Met28Val
ENST00000354171.12:c.82A>G	ENSP00000346103.7:p.Met28Val
ENST00000588919.5:c.1A>G	ENSP00000464989.3:p.Met1Val
ENST00000589115.5:c.82A>G	ENSP00000466872.2:p.Met28Val
ENST00000593032.5:c.1A>G	ENSP00000465828.3:p.Met1Val
ENST00000611653.4:c.1A>G	ENSP00000483655.1:p.Met1Val
ENST00000616066.4:c.82A>G	ENSP00000485000.1:p.Met28Val
NM_001039847.2:c.82A>G	NP_001034936.1:p.Met28Val
NM_002085.4:c.82A>G	NP_002076.2:p.Met28Val
NM_001039847.3:c.82A>G	NP_001034936.1:p.Met28Val
NM_001367832.1:c.1A>G	NP_001354761.1:p.Met1Val
NM_002085.5:c.82A>G MANE Select	NP_002076.2:p.Met28Val