Canonical Allele Identifier: CA1649863015
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875553_98875571delinsTGCTGCTCTGCAGAGTTGG , CM000668.2:g.98875553_98875571delinsTGCTGCTCTGCAGAGTTGG GRCh38
NC_000006.11:g.99323429_99323447delinsTGCTGCTCTGCAGAGTTGG , CM000668.1:g.99323429_99323447delinsTGCTGCTCTGCAGAGTTGG GRCh37
NC_000006.10:g.99430150_99430168delinsTGCTGCTCTGCAGAGTTGG NCBI36
NG_033903.1:g.77436_77454delinsCCAACTCTGCAGAGCAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1546_1564delinsCCAACTCTGCAGAGCAGCA MANE Select ENSP00000358247.1:p.Pro516=
ENST00000229971.2:c.1546_1564delinsCCAACTCTGCAGAGCAGCA ENSP00000229971.1:p.Pro516=
ENST00000369244.6:c.1546_1564delinsCCAACTCTGCAGAGCAGCA ENSP00000358247.1:p.Pro516=
NM_001278716.1:c.1546_1564delinsCCAACTCTGCAGAGCAGCA NP_001265645.1:p.Pro516=
NM_012160.4:c.1546_1564delinsCCAACTCTGCAGAGCAGCA NP_036292.2:p.Pro516=
NR_103836.1:n.1591_1609delinsCCAACTCTGCAGAGCAGCA
XM_005266930.1:c.1474_1492delinsCCAACTCTGCAGAGCAGCA XP_005266987.1:p.Pro492=
XM_005266930.3:c.1474_1492delinsCCAACTCTGCAGAGCAGCA XP_005266987.1:p.Pro492=
XM_017010726.1:c.1546_1564delinsCCAACTCTGCAGAGCAGCA XP_016866215.1:p.Pro516=
XM_017010727.2:c.1474_1492delinsCCAACTCTGCAGAGCAGCA XP_016866216.1:p.Pro492=
XM_017010728.1:c.820_838delinsCCAACTCTGCAGAGCAGCA XP_016866217.1:p.Pro274=
NM_001278716.2:c.1546_1564delinsCCAACTCTGCAGAGCAGCA MANE Select NP_001265645.1:p.Pro516=
NR_103836.2:n.1531_1549delinsCCAACTCTGCAGAGCAGCA
NM_012160.5:c.1546_1564delinsCCAACTCTGCAGAGCAGCA NP_036292.2:p.Pro516=