Canonical Allele Identifier: CA2588207859

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106499-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106499T>C , CM000681.2:g.1106499T>C	GRCh38
NC_000019.9:g.1106498T>C , CM000681.1:g.1106498T>C	GRCh37
NC_000019.8:g.1057498T>C	NCBI36
NG_050621.1:g.7574T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.673-41T>C	ENSP00000473614.3:n.673-41T>C
ENST00000593032.6:c.542-41T>C	ENSP00000465828.4:n.542-41T>C
ENST00000706713.1:c.556-41T>C	ENSP00000516510.1:n.556-41T>C
ENST00000706714.1:c.542-41T>C	ENSP00000516511.1:n.542-41T>C
ENST00000706715.1:c.178-41T>C	ENSP00000516512.1:n.178-41T>C
ENST00000354171.13:c.562-41T>C MANE Select	ENSP00000346103.7:n.562-41T>C
ENST00000589115.6:c.537-41T>C	ENSP00000466872.3:n.537-41T>C
ENST00000354171.12:c.562-41T>C	ENSP00000346103.7:n.562-41T>C
ENST00000585480.1:c.294+40T>C	ENSP00000467900.1:n.294+40T>C
ENST00000587648.5:c.442-41T>C	ENSP00000468349.1:n.442-41T>C
ENST00000588919.5:c.503-41T>C	ENSP00000464989.3:n.503-41T>C
ENST00000589115.5:c.537-41T>C	ENSP00000466872.2:n.537-41T>C
ENST00000592940.2:n.933-41T>C
ENST00000611653.4:c.481-41T>C	ENSP00000483655.1:n.481-41T>C
ENST00000616066.4:c.559-41T>C	ENSP00000485000.1:n.559-41T>C
ENST00000622390.4:c.670-41T>C	ENSP00000477503.1:n.670-41T>C
NM_001039847.2:c.584-41T>C	NP_001034936.1:n.584-41T>C
NM_001039848.2:c.673-41T>C	NP_001034937.1:n.673-41T>C
NM_002085.4:c.562-41T>C	NP_002076.2:n.562-41T>C
NM_001039848.3:c.673-41T>C	NP_001034937.1:n.673-41T>C
NM_001039847.3:c.584-41T>C	NP_001034936.1:n.584-41T>C
NM_001039848.4:c.673-41T>C	NP_001034937.1:n.673-41T>C
NM_001367832.1:c.481-41T>C	NP_001354761.1:n.481-41T>C
NM_002085.5:c.562-41T>C MANE Select	NP_002076.2:n.562-41T>C