Canonical Allele Identifier: CA2588207640

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106071-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106071T>C , CM000681.2:g.1106071T>C	GRCh38
NC_000019.9:g.1106070T>C , CM000681.1:g.1106070T>C	GRCh37
NC_000019.8:g.1057070T>C	NCBI36
NG_050621.1:g.7146T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-171T>C	ENSP00000473614.3:n.588-171T>C
ENST00000593032.6:c.396-110T>C	ENSP00000465828.4:n.396-110T>C
ENST00000706713.1:c.471-171T>C	ENSP00000516510.1:n.471-171T>C
ENST00000706714.1:c.396-110T>C	ENSP00000516511.1:n.396-110T>C
ENST00000706715.1:c.93-171T>C	ENSP00000516512.1:n.93-171T>C
ENST00000354171.13:c.477-171T>C MANE Select	ENSP00000346103.7:n.477-171T>C
ENST00000589115.6:c.476+262T>C	ENSP00000466872.3:n.476+262T>C
ENST00000354171.12:c.477-171T>C	ENSP00000346103.7:n.477-171T>C
ENST00000585480.1:c.210-171T>C	ENSP00000467900.1:n.210-171T>C
ENST00000587648.5:c.357-171T>C	ENSP00000468349.1:n.357-171T>C
ENST00000588919.5:c.396-171T>C	ENSP00000464989.3:n.396-171T>C
ENST00000589115.5:c.476+262T>C	ENSP00000466872.2:n.476+262T>C
ENST00000592940.2:n.677T>C
ENST00000593032.5:c.396-110T>C	ENSP00000465828.3:n.396-110T>C
ENST00000611653.4:c.396-171T>C	ENSP00000483655.1:n.396-171T>C
ENST00000616066.4:c.474-171T>C	ENSP00000485000.1:n.474-171T>C
ENST00000622390.4:c.585-171T>C	ENSP00000477503.1:n.585-171T>C
NM_001039847.2:c.477-171T>C	NP_001034936.1:n.477-171T>C
NM_001039848.2:c.588-171T>C	NP_001034937.1:n.588-171T>C
NM_002085.4:c.477-171T>C	NP_002076.2:n.477-171T>C
NM_001039848.3:c.588-171T>C	NP_001034937.1:n.588-171T>C
NM_001039847.3:c.477-171T>C	NP_001034936.1:n.477-171T>C
NM_001039848.4:c.588-171T>C	NP_001034937.1:n.588-171T>C
NM_001367832.1:c.396-171T>C	NP_001354761.1:n.396-171T>C
NM_002085.5:c.477-171T>C MANE Select	NP_002076.2:n.477-171T>C