Canonical Allele Identifier: CA1571013888

Gene: FBXL17

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.107945999_107946001delinsTAG , CM000667.2:g.107945999_107946001delinsTAG	GRCh38
NC_000005.9:g.107281700_107281702delinsTAG , CM000667.1:g.107281700_107281702delinsTAG	GRCh37
NC_000005.8:g.107309599_107309601delinsTAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496714.2:c.831-64822_831-64820delinsCTA
ENST00000542267.7:c.1823-64822_1823-64820delinsCTA MANE Select	ENSP00000437464.2:n.1823-64822_1823-64820delinsCTA
ENST00000359660.9:c.629-64822_629-64820delinsCTA	ENSP00000352683.4:n.629-64822_629-64820delinsCTA
ENST00000496714.1:c.629-64822_629-64820delinsCTA	ENSP00000418111.1:n.629-64822_629-64820delinsCTA
ENST00000542267.5:c.1823-64822_1823-64820delinsCTA	ENSP00000437464.1:n.1823-64822_1823-64820delinsCTA
ENST00000619412.4:c.1109-64822_1109-64820delinsCTA	ENSP00000481439.1:n.1109-64822_1109-64820delinsCTA
NM_001163315.2:c.1823-64822_1823-64820delinsCTA	NP_001156787.2:n.1823-64822_1823-64820delinsCTA
XM_005272048.3:c.1823-64822_1823-64820delinsCTA	XP_005272105.1:n.1823-64822_1823-64820delinsCTA
XM_005272048.4:c.1823-64822_1823-64820delinsCTA	XP_005272105.1:n.1823-64822_1823-64820delinsCTA
NM_001163315.3:c.1823-64822_1823-64820delinsCTA MANE Select	NP_001156787.2:n.1823-64822_1823-64820delinsCTA