Canonical Allele Identifier: CA2317518977
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2079618668

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103984_1103985insAA , CM000681.2:g.1103984_1103985insAA GRCh38
NC_000019.9:g.1103983_1103984insAA , CM000681.1:g.1103983_1103984insAA GRCh37
NC_000019.8:g.1054983_1054984insAA NCBI36
NG_050621.1:g.5059_5060insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706713.1:c.-60_-59insAA ENSP00000516510.1:n.-60_-59insAA
ENST00000354171.12:c.-60_-59insAA ENSP00000346103.7:n.-60_-59insAA
ENST00000616066.4:c.-60_-59insAA ENSP00000485000.1:n.-60_-59insAA
NM_001039847.2:c.-60_-59insAA NP_001034936.1:n.-60_-59insAA
NM_002085.4:c.-60_-59insAA NP_002076.2:n.-60_-59insAA