Canonical Allele Identifier: CA402940799

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106762A>C (hg19) ; chr19:g.1106763A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106763A>C , CM000681.2:g.1106763A>C	GRCh38
NC_000019.9:g.1106762A>C , CM000681.1:g.1106762A>C	GRCh37
NC_000019.8:g.1057762A>C	NCBI36
NG_050621.1:g.7838A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*191A>C	ENSP00000473614.3:n.*191A>C
ENST00000593032.6:c.765A>C	ENSP00000465828.4:p.Glu255Asp
ENST00000706713.1:c.*191A>C	ENSP00000516510.1:n.*191A>C
ENST00000706714.1:c.765A>C	ENSP00000516511.1:p.Glu255Asp
ENST00000706715.1:c.*191A>C	ENSP00000516512.1:n.*191A>C
ENST00000354171.13:c.*191A>C MANE Select	ENSP00000346103.7:n.*191A>C
ENST00000589115.6:c.*217A>C	ENSP00000466872.3:n.*217A>C
ENST00000354171.12:c.*191A>C	ENSP00000346103.7:n.*191A>C
ENST00000585480.1:c.485A>C	ENSP00000467900.1:p.Asn162Thr
ENST00000588919.5:c.726A>C	ENSP00000464989.3:p.Glu242Asp
ENST00000589115.5:c.*217A>C	ENSP00000466872.2:n.*217A>C
ENST00000592940.2:n.1156A>C
ENST00000611653.4:c.*191A>C	ENSP00000483655.1:n.*191A>C
ENST00000616066.4:c.*191A>C	ENSP00000485000.1:n.*191A>C
ENST00000622390.4:c.*191A>C	ENSP00000477503.1:n.*191A>C
NM_001039847.2:c.*123A>C	NP_001034936.1:n.*123A>C
NM_001039848.2:c.*191A>C	NP_001034937.1:n.*191A>C
NM_002085.4:c.*191A>C	NP_002076.2:n.*191A>C
NM_001039848.3:c.*191A>C	NP_001034937.1:n.*191A>C
NM_001039847.3:c.*123A>C	NP_001034936.1:n.*123A>C
NM_001039848.4:c.*191A>C	NP_001034937.1:n.*191A>C
NM_001367832.1:c.*191A>C	NP_001354761.1:n.*191A>C
NM_002085.5:c.*191A>C MANE Select	NP_002076.2:n.*191A>C