Canonical Allele Identifier: CA402934281

Gene: GPX4

Linked Data

• ClinVar Variation Id: 2319488
• ClinVar RCV Id: RCV002905634
• MyVariant Identifiers: chr19:g.1104115G>C (hg19) ; chr19:g.1104116G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104116G>C , CM000681.2:g.1104116G>C	GRCh38
NC_000019.9:g.1104115G>C , CM000681.1:g.1104115G>C	GRCh37
NC_000019.8:g.1055115G>C	NCBI36
NG_050621.1:g.5191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593032.6:c.-9G>C	ENSP00000465828.4:n.-9G>C
ENST00000706713.1:c.73G>C	ENSP00000516510.1:p.Ala25Pro
ENST00000706714.1:c.-9G>C	ENSP00000516511.1:n.-9G>C
ENST00000354171.13:c.73G>C MANE Select	ENSP00000346103.7:p.Ala25Pro
ENST00000589115.6:c.73G>C	ENSP00000466872.3:p.Ala25Pro
ENST00000354171.12:c.73G>C	ENSP00000346103.7:p.Ala25Pro
ENST00000588919.5:c.-9G>C	ENSP00000464989.3:n.-9G>C
ENST00000589115.5:c.73G>C	ENSP00000466872.2:p.Ala25Pro
ENST00000593032.5:c.-9G>C	ENSP00000465828.3:n.-9G>C
ENST00000611653.4:c.-9G>C	ENSP00000483655.1:n.-9G>C
ENST00000616066.4:c.73G>C	ENSP00000485000.1:p.Ala25Pro
NM_001039847.2:c.73G>C	NP_001034936.1:p.Ala25Pro
NM_002085.4:c.73G>C	NP_002076.2:p.Ala25Pro
NM_001039847.3:c.73G>C	NP_001034936.1:p.Ala25Pro
NM_001367832.1:c.-9G>C	NP_001354761.1:n.-9G>C
NM_002085.5:c.73G>C MANE Select	NP_002076.2:p.Ala25Pro