Canonical Allele Identifier: CA504694608

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105738-G-C
• MyVariant Identifiers: chr19:g.1105737G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105738G>C , CM000681.2:g.1105738G>C	GRCh38
NC_000019.9:g.1105737G>C , CM000681.1:g.1105737G>C	GRCh37
NC_000019.8:g.1056737G>C	NCBI36
NG_050621.1:g.6813G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.516G>C	ENSP00000473614.3:p.Val172=
ENST00000593032.6:c.324G>C	ENSP00000465828.4:p.Val108=
ENST00000706713.1:c.399G>C	ENSP00000516510.1:p.Val133=
ENST00000706714.1:c.324G>C	ENSP00000516511.1:p.Val108=
ENST00000706715.1:c.21G>C	ENSP00000516512.1:p.Val7=
ENST00000354171.13:c.405G>C MANE Select	ENSP00000346103.7:p.Val135=
ENST00000589115.6:c.405G>C	ENSP00000466872.3:p.Val135=
ENST00000354171.12:c.405G>C	ENSP00000346103.7:p.Val135=
ENST00000585362.6:c.516G>C	ENSP00000473614.2:p.Val172=
ENST00000585480.1:c.138G>C	ENSP00000467900.1:p.Val46=
ENST00000587648.5:c.285G>C	ENSP00000468349.1:p.Val95=
ENST00000588919.5:c.324G>C	ENSP00000464989.3:p.Val108=
ENST00000589115.5:c.405G>C	ENSP00000466872.2:p.Val135=
ENST00000592940.2:n.344G>C
ENST00000593032.5:c.324G>C	ENSP00000465828.3:p.Val108=
ENST00000611653.4:c.324G>C	ENSP00000483655.1:p.Val108=
ENST00000616066.4:c.402G>C	ENSP00000485000.1:p.Val134=
ENST00000622390.4:c.513G>C	ENSP00000477503.1:p.Val171=
NM_001039847.2:c.405G>C	NP_001034936.1:p.Val135=
NM_001039848.2:c.516G>C	NP_001034937.1:p.Val172=
NM_002085.4:c.405G>C	NP_002076.2:p.Val135=
NM_001039848.3:c.516G>C	NP_001034937.1:p.Val172=
NM_001039847.3:c.405G>C	NP_001034936.1:p.Val135=
NM_001039848.4:c.516G>C	NP_001034937.1:p.Val172=
NM_001367832.1:c.324G>C	NP_001354761.1:p.Val108=
NM_002085.5:c.405G>C MANE Select	NP_002076.2:p.Val135=