Canonical Allele Identifier: CA2576545187

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106643-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106643G>C , CM000681.2:g.1106643G>C	GRCh38
NC_000019.9:g.1106642G>C , CM000681.1:g.1106642G>C	GRCh37
NC_000019.8:g.1057642G>C	NCBI36
NG_050621.1:g.7718G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*71G>C	ENSP00000473614.3:n.*71G>C
ENST00000593032.6:c.645G>C	ENSP00000465828.4:p.Arg215=
ENST00000706713.1:c.*71G>C	ENSP00000516510.1:n.*71G>C
ENST00000706714.1:c.645G>C	ENSP00000516511.1:p.Arg215=
ENST00000706715.1:c.*71G>C	ENSP00000516512.1:n.*71G>C
ENST00000354171.13:c.*71G>C MANE Select	ENSP00000346103.7:n.*71G>C
ENST00000589115.6:c.*97G>C	ENSP00000466872.3:n.*97G>C
ENST00000354171.12:c.*71G>C	ENSP00000346103.7:n.*71G>C
ENST00000585480.1:c.365G>C	ENSP00000467900.1:p.Gly122Ala
ENST00000588919.5:c.606G>C	ENSP00000464989.3:p.Arg202=
ENST00000589115.5:c.*97G>C	ENSP00000466872.2:n.*97G>C
ENST00000592940.2:n.1036G>C
ENST00000611653.4:c.*71G>C	ENSP00000483655.1:n.*71G>C
ENST00000616066.4:c.*71G>C	ENSP00000485000.1:n.*71G>C
ENST00000622390.4:c.*71G>C	ENSP00000477503.1:n.*71G>C
NM_001039847.2:c.*3G>C	NP_001034936.1:n.*3G>C
NM_001039848.2:c.*71G>C	NP_001034937.1:n.*71G>C
NM_002085.4:c.*71G>C	NP_002076.2:n.*71G>C
NM_001039848.3:c.*71G>C	NP_001034937.1:n.*71G>C
NM_001039847.3:c.*3G>C	NP_001034936.1:n.*3G>C
NM_001039848.4:c.*71G>C	NP_001034937.1:n.*71G>C
NM_001367832.1:c.*71G>C	NP_001354761.1:n.*71G>C
NM_002085.5:c.*71G>C MANE Select	NP_002076.2:n.*71G>C