Canonical Allele Identifier: CA402937671

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105787A>T (hg19) ; chr19:g.1105788A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105788A>T , CM000681.2:g.1105788A>T	GRCh38
NC_000019.9:g.1105787A>T , CM000681.1:g.1105787A>T	GRCh37
NC_000019.8:g.1056787A>T	NCBI36
NG_050621.1:g.6863A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.566A>T	ENSP00000473614.3:p.Lys189Met
ENST00000593032.6:c.374A>T	ENSP00000465828.4:p.Lys125Met
ENST00000706713.1:c.449A>T	ENSP00000516510.1:p.Lys150Met
ENST00000706714.1:c.374A>T	ENSP00000516511.1:p.Lys125Met
ENST00000706715.1:c.71A>T	ENSP00000516512.1:p.Lys24Met
ENST00000354171.13:c.455A>T MANE Select	ENSP00000346103.7:p.Lys152Met
ENST00000589115.6:c.455A>T	ENSP00000466872.3:p.Lys152Met
ENST00000354171.12:c.455A>T	ENSP00000346103.7:p.Lys152Met
ENST00000585480.1:c.188A>T	ENSP00000467900.1:p.Lys63Met
ENST00000587648.5:c.335A>T	ENSP00000468349.1:p.Lys112Met
ENST00000588919.5:c.374A>T	ENSP00000464989.3:p.Lys125Met
ENST00000589115.5:c.455A>T	ENSP00000466872.2:p.Lys152Met
ENST00000592940.2:n.394A>T
ENST00000593032.5:c.374A>T	ENSP00000465828.3:p.Lys125Met
ENST00000611653.4:c.374A>T	ENSP00000483655.1:p.Lys125Met
ENST00000616066.4:c.452A>T	ENSP00000485000.1:p.Lys151Met
ENST00000622390.4:c.563A>T	ENSP00000477503.1:p.Lys188Met
NM_001039847.2:c.455A>T	NP_001034936.1:p.Lys152Met
NM_001039848.2:c.566A>T	NP_001034937.1:p.Lys189Met
NM_002085.4:c.455A>T	NP_002076.2:p.Lys152Met
NM_001039848.3:c.566A>T	NP_001034937.1:p.Lys189Met
NM_001039847.3:c.455A>T	NP_001034936.1:p.Lys152Met
NM_001039848.4:c.566A>T	NP_001034937.1:p.Lys189Met
NM_001367832.1:c.374A>T	NP_001354761.1:p.Lys125Met
NM_002085.5:c.455A>T MANE Select	NP_002076.2:p.Lys152Met