Canonical Allele Identifier: CA3933436
Community Standard Title: NM_001278716.2(FBXL4):c.1464A>G (p.Arg488=)
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875653T>C , CM000668.2:g.98875653T>C GRCh38
NC_000006.11:g.99323529T>C , CM000668.1:g.99323529T>C GRCh37
NC_000006.10:g.99430250T>C NCBI36
NG_033903.1:g.77354A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001278716.2:c.1464A>G MANE Select NP_001265645.1:p.Arg488=
ENST00000369244.7:c.1464A>G MANE Select ENSP00000358247.1:p.Arg488=
NM_001278716.1:c.1464A>G NP_001265645.1:p.Arg488=
NM_012160.4:c.1464A>G NP_036292.2:p.Arg488=
NM_012160.5:c.1464A>G NP_036292.2:p.Arg488=
NR_103836.1:n.1509A>G
NR_103836.2:n.1449A>G
ENST00000229971.2:c.1464A>G ENSP00000229971.1:p.Arg488=
ENST00000369244.6:c.1464A>G ENSP00000358247.1:p.Arg488=
XM_005266930.1:c.1392A>G XP_005266987.1:p.Arg464=
XM_005266930.3:c.1392A>G XP_005266987.1:p.Arg464=
XM_017010726.1:c.1464A>G XP_016866215.1:p.Arg488=
XM_017010727.2:c.1392A>G XP_016866216.1:p.Arg464=
XM_017010728.1:c.738A>G XP_016866217.1:p.Arg246=