Canonical Allele Identifier: CA2588207878

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106533-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106533_1106534insAG , CM000681.2:g.1106533_1106534insAG	GRCh38
NC_000019.9:g.1106532_1106533insAG , CM000681.1:g.1106532_1106533insAG	GRCh37
NC_000019.8:g.1057532_1057533insAG	NCBI36
NG_050621.1:g.7608_7609insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.673-7_673-6insAG	ENSP00000473614.3:n.673-7_673-6insAG
ENST00000593032.6:c.542-7_542-6insAG	ENSP00000465828.4:n.542-7_542-6insAG
ENST00000706713.1:c.556-7_556-6insAG	ENSP00000516510.1:n.556-7_556-6insAG
ENST00000706714.1:c.542-7_542-6insAG	ENSP00000516511.1:n.542-7_542-6insAG
ENST00000706715.1:c.178-7_178-6insAG	ENSP00000516512.1:n.178-7_178-6insAG
ENST00000354171.13:c.562-7_562-6insAG MANE Select	ENSP00000346103.7:n.562-7_562-6insAG
ENST00000589115.6:c.537-7_537-6insAG	ENSP00000466872.3:n.537-7_537-6insAG
ENST00000354171.12:c.562-7_562-6insAG	ENSP00000346103.7:n.562-7_562-6insAG
ENST00000585480.1:c.295-40_295-39insAG	ENSP00000467900.1:n.295-40_295-39insAG
ENST00000587648.5:c.442-7_442-6insAG	ENSP00000468349.1:n.442-7_442-6insAG
ENST00000588919.5:c.503-7_503-6insAG	ENSP00000464989.3:n.503-7_503-6insAG
ENST00000589115.5:c.537-7_537-6insAG	ENSP00000466872.2:n.537-7_537-6insAG
ENST00000592940.2:n.933-7_933-6insAG
ENST00000611653.4:c.481-7_481-6insAG	ENSP00000483655.1:n.481-7_481-6insAG
ENST00000616066.4:c.559-7_559-6insAG	ENSP00000485000.1:n.559-7_559-6insAG
ENST00000622390.4:c.670-7_670-6insAG	ENSP00000477503.1:n.670-7_670-6insAG
NM_001039847.2:c.584-7_584-6insAG	NP_001034936.1:n.584-7_584-6insAG
NM_001039848.2:c.673-7_673-6insAG	NP_001034937.1:n.673-7_673-6insAG
NM_002085.4:c.562-7_562-6insAG	NP_002076.2:n.562-7_562-6insAG
NM_001039848.3:c.673-7_673-6insAG	NP_001034937.1:n.673-7_673-6insAG
NM_001039847.3:c.584-7_584-6insAG	NP_001034936.1:n.584-7_584-6insAG
NM_001039848.4:c.673-7_673-6insAG	NP_001034937.1:n.673-7_673-6insAG
NM_001367832.1:c.481-7_481-6insAG	NP_001354761.1:n.481-7_481-6insAG
NM_002085.5:c.562-7_562-6insAG MANE Select	NP_002076.2:n.562-7_562-6insAG