Canonical Allele Identifier: CA402940790

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106758G>C (hg19) ; chr19:g.1106759G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106759G>C , CM000681.2:g.1106759G>C	GRCh38
NC_000019.9:g.1106758G>C , CM000681.1:g.1106758G>C	GRCh37
NC_000019.8:g.1057758G>C	NCBI36
NG_050621.1:g.7834G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*187G>C	ENSP00000473614.3:n.*187G>C
ENST00000593032.6:c.761G>C	ENSP00000465828.4:p.Trp254Ser
ENST00000706713.1:c.*187G>C	ENSP00000516510.1:n.*187G>C
ENST00000706714.1:c.761G>C	ENSP00000516511.1:p.Trp254Ser
ENST00000706715.1:c.*187G>C	ENSP00000516512.1:n.*187G>C
ENST00000354171.13:c.*187G>C MANE Select	ENSP00000346103.7:n.*187G>C
ENST00000589115.6:c.*213G>C	ENSP00000466872.3:n.*213G>C
ENST00000354171.12:c.*187G>C	ENSP00000346103.7:n.*187G>C
ENST00000585480.1:c.481G>C	ENSP00000467900.1:p.Gly161Arg
ENST00000588919.5:c.722G>C	ENSP00000464989.3:p.Trp241Ser
ENST00000589115.5:c.*213G>C	ENSP00000466872.2:n.*213G>C
ENST00000592940.2:n.1152G>C
ENST00000611653.4:c.*187G>C	ENSP00000483655.1:n.*187G>C
ENST00000616066.4:c.*187G>C	ENSP00000485000.1:n.*187G>C
ENST00000622390.4:c.*187G>C	ENSP00000477503.1:n.*187G>C
NM_001039847.2:c.*119G>C	NP_001034936.1:n.*119G>C
NM_001039848.2:c.*187G>C	NP_001034937.1:n.*187G>C
NM_002085.4:c.*187G>C	NP_002076.2:n.*187G>C
NM_001039848.3:c.*187G>C	NP_001034937.1:n.*187G>C
NM_001039847.3:c.*119G>C	NP_001034936.1:n.*119G>C
NM_001039848.4:c.*187G>C	NP_001034937.1:n.*187G>C
NM_001367832.1:c.*187G>C	NP_001354761.1:n.*187G>C
NM_002085.5:c.*187G>C MANE Select	NP_002076.2:n.*187G>C