Canonical Allele Identifier: CA397762506

Gene: FBXO39

Linked Data

• MyVariant Identifiers: chr17:g.6684067A>T (hg19) ; chr17:g.6780748A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6780748A>T , CM000679.2:g.6780748A>T	GRCh38
NC_000017.10:g.6684067A>T , CM000679.1:g.6684067A>T	GRCh37
NC_000017.9:g.6624791A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321535.5:c.880A>T MANE Select	ENSP00000321386.4:p.Lys294Ter
ENST00000321535.4:c.880A>T	ENSP00000321386.4:p.Lys294Ter
NM_153230.2:c.880A>T	NP_694962.1:p.Lys294Ter
XM_011523697.1:c.880A>T	XP_011521999.1:p.Lys294Ter
XR_243544.3:n.1058A>T
NM_153230.3:c.880A>T MANE Select	NP_694962.1:p.Lys294Ter