Canonical Allele Identifier: CA2245514012
Gene: FBXO39 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780859_6780860delinsGA , CM000679.2:g.6780859_6780860delinsGA GRCh38
NC_000017.10:g.6684178_6684179delinsGA , CM000679.1:g.6684178_6684179delinsGA GRCh37
NC_000017.9:g.6624902_6624903delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.991_992delinsGA MANE Select ENSP00000321386.4:p.Asp331=
ENST00000321535.4:c.991_992delinsGA ENSP00000321386.4:p.Asp331=
NM_153230.2:c.991_992delinsGA NP_694962.1:p.Asp331=
XM_011523697.1:c.991_992delinsGA XP_011521999.1:p.Asp331=
XR_243544.3:n.1169_1170delinsGA
NM_153230.3:c.991_992delinsGA MANE Select NP_694962.1:p.Asp331=
Search 100 bp 5'
Search 100 bp 3'