Canonical Allele Identifier: CA2317518935
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2079618132

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103948del , CM000681.2:g.1103948del GRCh38
NC_000019.9:g.1103947del , CM000681.1:g.1103947del GRCh37
NC_000019.8:g.1054947del NCBI36
NG_050621.1:g.5023del

Transcript Alleles

HGVS Amino-acid change
ENST00000354171.12:c.-96del ENSP00000346103.7:n.-96del
ENST00000616066.4:c.-96del ENSP00000485000.1:n.-96del
NM_001039847.2:c.-96del NP_001034936.1:n.-96del
NM_002085.4:c.-96del NP_002076.2:n.-96del