Canonical Allele Identifier: CA1649862553

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875294C= , CM000668.2:g.98875294C=	GRCh38
NC_000006.11:g.99323170C= , CM000668.1:g.99323170C=	GRCh37
NC_000006.10:g.99429891C=	NCBI36
NG_033903.1:g.77713G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+121G= MANE Select	ENSP00000358247.1:n.1702+121G=
ENST00000229971.2:c.1702+121G=	ENSP00000229971.1:n.1702+121G=
ENST00000369244.6:c.1702+121G=	ENSP00000358247.1:n.1702+121G=
NM_001278716.1:c.1702+121G=	NP_001265645.1:n.1702+121G=
NM_012160.4:c.1702+121G=	NP_036292.2:n.1702+121G=
NR_103836.1:n.1747+121G=
XM_005266930.1:c.1630+121G=	XP_005266987.1:n.1630+121G=
XM_005266930.3:c.1630+121G=	XP_005266987.1:n.1630+121G=
XM_017010726.1:c.1702+121G=	XP_016866215.1:n.1702+121G=
XM_017010727.2:c.1630+121G=	XP_016866216.1:n.1630+121G=
XM_017010728.1:c.976+121G=	XP_016866217.1:n.976+121G=
NM_001278716.2:c.1702+121G= MANE Select	NP_001265645.1:n.1702+121G=
NR_103836.2:n.1687+121G=
NM_012160.5:c.1702+121G=	NP_036292.2:n.1702+121G=