Canonical Allele Identifier: CA1590036279

Gene: FBXO38

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148425185_148425187delinsCTG , CM000667.2:g.148425185_148425187delinsCTG	GRCh38
NC_000005.9:g.147804748_147804750delinsCTG , CM000667.1:g.147804748_147804750delinsCTG	GRCh37
NC_000005.8:g.147784941_147784943delinsCTG	NCBI36
NG_033871.1:g.46251_46253delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340253.10:c.1739-337_1739-335delinsCTG MANE Select	ENSP00000342023.6:n.1739-337_1739-335delinsCTG
ENST00000296701.10:c.1739-337_1739-335delinsCTG	ENSP00000296701.6:n.1739-337_1739-335delinsCTG
ENST00000340253.9:c.1739-337_1739-335delinsCTG	ENSP00000342023.5:n.1739-337_1739-335delinsCTG
ENST00000394370.7:c.1739-337_1739-335delinsCTG	ENSP00000377895.3:n.1739-337_1739-335delinsCTG
ENST00000513826.1:c.1739-337_1739-335delinsCTG	ENSP00000426410.1:n.1739-337_1739-335delinsCTG
ENST00000514832.1:n.370-337_370-335delinsCTG
NM_001271723.1:c.1739-337_1739-335delinsCTG	NP_001258652.1:n.1739-337_1739-335delinsCTG
NM_030793.4:c.1739-337_1739-335delinsCTG	NP_110420.3:n.1739-337_1739-335delinsCTG
XM_005268513.1:c.1739-337_1739-335delinsCTG	XP_005268570.1:n.1739-337_1739-335delinsCTG
XM_006714797.1:c.1739-337_1739-335delinsCTG	XP_006714860.1:n.1739-337_1739-335delinsCTG
XM_011537683.1:c.641-337_641-335delinsCTG	XP_011535985.1:n.641-337_641-335delinsCTG
XM_011537684.1:c.539-337_539-335delinsCTG	XP_011535986.1:n.539-337_539-335delinsCTG
NM_205836.2:c.1739-337_1739-335delinsCTG	NP_995308.1:n.1739-337_1739-335delinsCTG
XM_006714797.2:c.1739-337_1739-335delinsCTG	XP_006714860.1:n.1739-337_1739-335delinsCTG
XM_011537684.3:c.539-337_539-335delinsCTG	XP_011535986.1:n.539-337_539-335delinsCTG
XM_017009899.1:c.641-337_641-335delinsCTG	XP_016865388.1:n.641-337_641-335delinsCTG
XM_017009900.2:c.539-337_539-335delinsCTG	XP_016865389.1:n.539-337_539-335delinsCTG
XM_017009901.2:c.641-337_641-335delinsCTG	XP_016865390.1:n.641-337_641-335delinsCTG
XM_017009902.2:c.539-337_539-335delinsCTG	XP_016865391.1:n.539-337_539-335delinsCTG
XM_024446223.1:c.1739-337_1739-335delinsCTG	XP_024301991.1:n.1739-337_1739-335delinsCTG
XR_001742284.1:n.1885-337_1885-335delinsCTG
NM_030793.5:c.1739-337_1739-335delinsCTG	NP_110420.3:n.1739-337_1739-335delinsCTG
NM_205836.3:c.1739-337_1739-335delinsCTG MANE Select	NP_995308.1:n.1739-337_1739-335delinsCTG
NM_001271723.2:c.1739-337_1739-335delinsCTG	NP_001258652.1:n.1739-337_1739-335delinsCTG