Canonical Allele Identifier: CA1649907583

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926683T= , CM000668.2:g.98926683T=	GRCh38
NC_000006.11:g.99374559T= , CM000668.1:g.99374559T=	GRCh37
NC_000006.10:g.99481280T=	NCBI36
NG_033903.1:g.26324A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.306A= MANE Select	ENSP00000358247.1:p.Thr102=
ENST00000229971.2:c.306A=	ENSP00000229971.1:p.Thr102=
ENST00000369244.6:c.306A=	ENSP00000358247.1:p.Thr102=
NM_001278716.1:c.306A=	NP_001265645.1:p.Thr102=
NM_012160.4:c.306A=	NP_036292.2:p.Thr102=
NR_103836.1:n.697A=
NR_103837.1:n.697A=
XM_005266930.1:c.306A=	XP_005266987.1:p.Thr102=
XM_011535748.1:c.306A=	XP_011534050.1:p.Thr102=
XM_005266930.3:c.306A=	XP_005266987.1:p.Thr102=
XM_011535748.3:c.306A=	XP_011534050.1:p.Thr102=
XM_017010726.1:c.306A=	XP_016866215.1:p.Thr102=
XM_017010727.2:c.306A=	XP_016866216.1:p.Thr102=
XM_017010728.1:c.-497A=	XP_016866217.1:n.-497A=
NM_001278716.2:c.306A= MANE Select	NP_001265645.1:p.Thr102=
NR_103836.2:n.637A=
NR_103837.2:n.637A=
NM_012160.5:c.306A=	NP_036292.2:p.Thr102=