Canonical Allele Identifier: CA1649907824

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926838C= , CM000668.2:g.98926838C=	GRCh38
NC_000006.11:g.99374714C= , CM000668.1:g.99374714C=	GRCh37
NC_000006.10:g.99481435C=	NCBI36
NG_033903.1:g.26169G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369244.7:c.151G= MANE Select	ENSP00000358247.1:p.Val51=
ENST00000229971.2:c.151G=	ENSP00000229971.1:p.Val51=
ENST00000369244.6:c.151G=	ENSP00000358247.1:p.Val51=
NM_001278716.1:c.151G=	NP_001265645.1:p.Val51=
NM_012160.4:c.151G=	NP_036292.2:p.Val51=
NR_103836.1:n.542G=
NR_103837.1:n.542G=
XM_005266930.1:c.151G=	XP_005266987.1:p.Val51=
XM_011535748.1:c.151G=	XP_011534050.1:p.Val51=
XM_005266930.3:c.151G=	XP_005266987.1:p.Val51=
XM_011535748.3:c.151G=	XP_011534050.1:p.Val51=
XM_017010726.1:c.151G=	XP_016866215.1:p.Val51=
XM_017010727.2:c.151G=	XP_016866216.1:p.Val51=
XM_017010728.1:c.-652G=	XP_016866217.1:n.-652G=
NM_001278716.2:c.151G= MANE Select	NP_001265645.1:p.Val51=
NR_103836.2:n.482G=
NR_103837.2:n.482G=
NM_012160.5:c.151G=	NP_036292.2:p.Val51=