Canonical Allele Identifier: CA402937638

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105773G>C (hg19) ; chr19:g.1105774G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105774G>C , CM000681.2:g.1105774G>C	GRCh38
NC_000019.9:g.1105773G>C , CM000681.1:g.1105773G>C	GRCh37
NC_000019.8:g.1056773G>C	NCBI36
NG_050621.1:g.6849G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.552G>C	ENSP00000473614.3:p.Met184Ile
ENST00000593032.6:c.360G>C	ENSP00000465828.4:p.Met120Ile
ENST00000706713.1:c.435G>C	ENSP00000516510.1:p.Met145Ile
ENST00000706714.1:c.360G>C	ENSP00000516511.1:p.Met120Ile
ENST00000706715.1:c.57G>C	ENSP00000516512.1:p.Met19Ile
ENST00000354171.13:c.441G>C MANE Select	ENSP00000346103.7:p.Met147Ile
ENST00000589115.6:c.441G>C	ENSP00000466872.3:p.Met147Ile
ENST00000354171.12:c.441G>C	ENSP00000346103.7:p.Met147Ile
ENST00000585480.1:c.174G>C	ENSP00000467900.1:p.Met58Ile
ENST00000587648.5:c.321G>C	ENSP00000468349.1:p.Met107Ile
ENST00000588919.5:c.360G>C	ENSP00000464989.3:p.Met120Ile
ENST00000589115.5:c.441G>C	ENSP00000466872.2:p.Met147Ile
ENST00000592940.2:n.380G>C
ENST00000593032.5:c.360G>C	ENSP00000465828.3:p.Met120Ile
ENST00000611653.4:c.360G>C	ENSP00000483655.1:p.Met120Ile
ENST00000616066.4:c.438G>C	ENSP00000485000.1:p.Met146Ile
ENST00000622390.4:c.549G>C	ENSP00000477503.1:p.Met183Ile
NM_001039847.2:c.441G>C	NP_001034936.1:p.Met147Ile
NM_001039848.2:c.552G>C	NP_001034937.1:p.Met184Ile
NM_002085.4:c.441G>C	NP_002076.2:p.Met147Ile
NM_001039848.3:c.552G>C	NP_001034937.1:p.Met184Ile
NM_001039847.3:c.441G>C	NP_001034936.1:p.Met147Ile
NM_001039848.4:c.552G>C	NP_001034937.1:p.Met184Ile
NM_001367832.1:c.360G>C	NP_001354761.1:p.Met120Ile
NM_002085.5:c.441G>C MANE Select	NP_002076.2:p.Met147Ile