Canonical Allele Identifier: CA15411081

Gene: FBXL17

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.107945920C>T , CM000667.2:g.107945920C>T	GRCh38
NC_000005.9:g.107281621C>T , CM000667.1:g.107281621C>T	GRCh37
NC_000005.8:g.107309520C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001163315.3:c.1823-64741G>A MANE Select	NP_001156787.2:n.1823-64741G>A
ENST00000542267.7:c.1823-64741G>A MANE Select	ENSP00000437464.2:n.1823-64741G>A
NM_001163315.2:c.1823-64741G>A	NP_001156787.2:n.1823-64741G>A
ENST00000359660.9:c.629-64741G>A	ENSP00000352683.4:n.629-64741G>A
ENST00000496714.1:c.629-64741G>A	ENSP00000418111.1:n.629-64741G>A
ENST00000496714.2:c.831-64741G>A
ENST00000542267.5:c.1823-64741G>A	ENSP00000437464.1:n.1823-64741G>A
ENST00000619412.4:c.1109-64741G>A	ENSP00000481439.1:n.1109-64741G>A
XM_005272048.3:c.1823-64741G>A	XP_005272105.1:n.1823-64741G>A
XM_005272048.4:c.1823-64741G>A	XP_005272105.1:n.1823-64741G>A