Canonical Allele Identifier: CA365086176
Gene: FBXL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875414C>T , CM000668.2:g.98875414C>T GRCh38
NC_000006.11:g.99323290C>T , CM000668.1:g.99323290C>T GRCh37
NC_000006.10:g.99430011C>T NCBI36
NG_033903.1:g.77593G>A

Transcript Alleles

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