Canonical Allele Identifier: CA1571013844
Gene: FBXL17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107945920_107945927delinsCCATTTTT , CM000667.2:g.107945920_107945927delinsCCATTTTT GRCh38
NC_000005.9:g.107281621_107281628delinsCCATTTTT , CM000667.1:g.107281621_107281628delinsCCATTTTT GRCh37
NC_000005.8:g.107309520_107309527delinsCCATTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496714.2:c.831-64748_831-64741delinsAAAAATGG
ENST00000542267.7:c.1823-64748_1823-64741delinsAAAAATGG MANE Select ENSP00000437464.2:n.1823-64748_1823-64741delinsAAAAATGG
ENST00000359660.9:c.629-64748_629-64741delinsAAAAATGG ENSP00000352683.4:n.629-64748_629-64741delinsAAAAATGG
ENST00000496714.1:c.629-64748_629-64741delinsAAAAATGG ENSP00000418111.1:n.629-64748_629-64741delinsAAAAATGG
ENST00000542267.5:c.1823-64748_1823-64741delinsAAAAATGG ENSP00000437464.1:n.1823-64748_1823-64741delinsAAAAATGG
ENST00000619412.4:c.1109-64748_1109-64741delinsAAAAATGG ENSP00000481439.1:n.1109-64748_1109-64741delinsAAAAATGG
NM_001163315.2:c.1823-64748_1823-64741delinsAAAAATGG NP_001156787.2:n.1823-64748_1823-64741delinsAAAAATGG
XM_005272048.3:c.1823-64748_1823-64741delinsAAAAATGG XP_005272105.1:n.1823-64748_1823-64741delinsAAAAATGG
XM_005272048.4:c.1823-64748_1823-64741delinsAAAAATGG XP_005272105.1:n.1823-64748_1823-64741delinsAAAAATGG
NM_001163315.3:c.1823-64748_1823-64741delinsAAAAATGG MANE Select NP_001156787.2:n.1823-64748_1823-64741delinsAAAAATGG