Canonical Allele Identifier: CA2695206824

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875610_98875611insGA , CM000668.2:g.98875610_98875611insGA	GRCh38
NC_000006.11:g.99323486_99323487insGA , CM000668.1:g.99323486_99323487insGA	GRCh37
NC_000006.10:g.99430207_99430208insGA	NCBI36
NG_033903.1:g.77396_77397insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1506_1507insTC MANE Select	ENSP00000358247.1:p.Gly503SerfsTer?
ENST00000229971.2:c.1506_1507insTC	ENSP00000229971.1:p.Gly503SerfsTer?
ENST00000369244.6:c.1506_1507insTC	ENSP00000358247.1:p.Gly503SerfsTer?
NM_001278716.1:c.1506_1507insTC	NP_001265645.1:p.Gly503SerfsTer?
NM_012160.4:c.1506_1507insTC	NP_036292.2:p.Gly503SerfsTer?
NR_103836.1:n.1551_1552insTC
XM_005266930.1:c.1434_1435insTC	XP_005266987.1:p.Gly479SerfsTer?
XM_005266930.3:c.1434_1435insTC	XP_005266987.1:p.Gly479SerfsTer?
XM_017010726.1:c.1506_1507insTC	XP_016866215.1:p.Gly503SerfsTer?
XM_017010727.2:c.1434_1435insTC	XP_016866216.1:p.Gly479SerfsTer?
XM_017010728.1:c.780_781insTC	XP_016866217.1:p.Gly261SerfsTer?
NM_001278716.2:c.1506_1507insTC MANE Select	NP_001265645.1:p.Gly503SerfsTer?
NR_103836.2:n.1491_1492insTC
NM_012160.5:c.1506_1507insTC	NP_036292.2:p.Gly503SerfsTer?