Canonical Allele Identifier: CA913015497

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106304-T-C
• MyVariant Identifiers: chr19:g.1106303T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106304T>C , CM000681.2:g.1106304T>C	GRCh38
NC_000019.9:g.1106303T>C , CM000681.1:g.1106303T>C	GRCh37
NC_000019.8:g.1057303T>C	NCBI36
NG_050621.1:g.7379T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.612+38T>C	ENSP00000473614.3:n.612+38T>C
ENST00000593032.6:c.481+38T>C	ENSP00000465828.4:n.481+38T>C
ENST00000706713.1:c.495+38T>C	ENSP00000516510.1:n.495+38T>C
ENST00000706714.1:c.481+38T>C	ENSP00000516511.1:n.481+38T>C
ENST00000706715.1:c.117+38T>C	ENSP00000516512.1:n.117+38T>C
ENST00000354171.13:c.501+38T>C MANE Select	ENSP00000346103.7:n.501+38T>C
ENST00000589115.6:c.477-96T>C	ENSP00000466872.3:n.477-96T>C
ENST00000354171.12:c.501+38T>C	ENSP00000346103.7:n.501+38T>C
ENST00000585480.1:c.234+38T>C	ENSP00000467900.1:n.234+38T>C
ENST00000587648.5:c.381+38T>C	ENSP00000468349.1:n.381+38T>C
ENST00000588919.5:c.420+38T>C	ENSP00000464989.3:n.420+38T>C
ENST00000589115.5:c.477-96T>C	ENSP00000466872.2:n.477-96T>C
ENST00000592940.2:n.872+38T>C
ENST00000593032.5:c.481+38T>C	ENSP00000465828.3:n.481+38T>C
ENST00000611653.4:c.420+38T>C	ENSP00000483655.1:n.420+38T>C
ENST00000616066.4:c.498+38T>C	ENSP00000485000.1:n.498+38T>C
ENST00000622390.4:c.609+38T>C	ENSP00000477503.1:n.609+38T>C
NM_001039847.2:c.501+38T>C	NP_001034936.1:n.501+38T>C
NM_001039848.2:c.612+38T>C	NP_001034937.1:n.612+38T>C
NM_002085.4:c.501+38T>C	NP_002076.2:n.501+38T>C
NM_001039848.3:c.612+38T>C	NP_001034937.1:n.612+38T>C
NM_001039847.3:c.501+38T>C	NP_001034936.1:n.501+38T>C
NM_001039848.4:c.612+38T>C	NP_001034937.1:n.612+38T>C
NM_001367832.1:c.420+38T>C	NP_001354761.1:n.420+38T>C
NM_002085.5:c.501+38T>C MANE Select	NP_002076.2:n.501+38T>C