Canonical Allele Identifier: CA16021016

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98917570T>A , CM000668.2:g.98917570T>A	GRCh38
NC_000006.11:g.99365446T>A , CM000668.1:g.99365446T>A	GRCh37
NC_000006.10:g.99472167T>A	NCBI36
NG_033903.1:g.35437A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001278716.2:c.662A>T MANE Select	NP_001265645.1:p.Asp221Val
ENST00000369244.7:c.662A>T MANE Select	ENSP00000358247.1:p.Asp221Val
NM_001278716.1:c.662A>T	NP_001265645.1:p.Asp221Val
NM_012160.4:c.662A>T	NP_036292.2:p.Asp221Val
NM_012160.5:c.662A>T	NP_036292.2:p.Asp221Val
NR_103836.1:n.903+8907A>T
NR_103836.2:n.843+8907A>T
NR_103837.1:n.903+8907A>T
NR_103837.2:n.843+8907A>T
ENST00000229971.2:c.662A>T	ENSP00000229971.1:p.Asp221Val
ENST00000369244.6:c.662A>T	ENSP00000358247.1:p.Asp221Val
XM_005266930.1:c.662A>T	XP_005266987.1:p.Asp221Val
XM_005266930.3:c.662A>T	XP_005266987.1:p.Asp221Val
XM_011535748.1:c.662A>T	XP_011534050.1:p.Asp221Val
XM_011535748.3:c.662A>T	XP_011534050.1:p.Asp221Val
XM_017010726.1:c.662A>T	XP_016866215.1:p.Asp221Val
XM_017010727.2:c.662A>T	XP_016866216.1:p.Asp221Val
XM_017010728.1:c.-65A>T	XP_016866217.1:n.-65A>T