Canonical Allele Identifier: CA504694635

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105759-G-T
• MyVariant Identifiers: chr19:g.1105758G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105759G>T , CM000681.2:g.1105759G>T	GRCh38
NC_000019.9:g.1105758G>T , CM000681.1:g.1105758G>T	GRCh37
NC_000019.8:g.1056758G>T	NCBI36
NG_050621.1:g.6834G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.537G>T	ENSP00000473614.3:p.Pro179=
ENST00000593032.6:c.345G>T	ENSP00000465828.4:p.Pro115=
ENST00000706713.1:c.420G>T	ENSP00000516510.1:p.Pro140=
ENST00000706714.1:c.345G>T	ENSP00000516511.1:p.Pro115=
ENST00000706715.1:c.42G>T	ENSP00000516512.1:p.Pro14=
ENST00000354171.13:c.426G>T MANE Select	ENSP00000346103.7:p.Pro142=
ENST00000589115.6:c.426G>T	ENSP00000466872.3:p.Pro142=
ENST00000354171.12:c.426G>T	ENSP00000346103.7:p.Pro142=
ENST00000585362.6:c.537G>T	ENSP00000473614.2:p.Pro179=
ENST00000585480.1:c.159G>T	ENSP00000467900.1:p.Pro53=
ENST00000587648.5:c.306G>T	ENSP00000468349.1:p.Pro102=
ENST00000588919.5:c.345G>T	ENSP00000464989.3:p.Pro115=
ENST00000589115.5:c.426G>T	ENSP00000466872.2:p.Pro142=
ENST00000592940.2:n.365G>T
ENST00000593032.5:c.345G>T	ENSP00000465828.3:p.Pro115=
ENST00000611653.4:c.345G>T	ENSP00000483655.1:p.Pro115=
ENST00000616066.4:c.423G>T	ENSP00000485000.1:p.Pro141=
ENST00000622390.4:c.534G>T	ENSP00000477503.1:p.Pro178=
NM_001039847.2:c.426G>T	NP_001034936.1:p.Pro142=
NM_001039848.2:c.537G>T	NP_001034937.1:p.Pro179=
NM_002085.4:c.426G>T	NP_002076.2:p.Pro142=
NM_001039848.3:c.537G>T	NP_001034937.1:p.Pro179=
NM_001039847.3:c.426G>T	NP_001034936.1:p.Pro142=
NM_001039848.4:c.537G>T	NP_001034937.1:p.Pro179=
NM_001367832.1:c.345G>T	NP_001354761.1:p.Pro115=
NM_002085.5:c.426G>T MANE Select	NP_002076.2:p.Pro142=