Canonical Allele Identifier: CA2679757755
Gene: FBXL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875490dup , CM000668.2:g.98875490dup GRCh38
NC_000006.11:g.99323366dup , CM000668.1:g.99323366dup GRCh37
NC_000006.10:g.99430087dup NCBI36
NG_033903.1:g.77518dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1628dup MANE Select ENSP00000358247.1:p.Asn543LysfsTer2
ENST00000229971.2:c.1628dup ENSP00000229971.1:p.Asn543LysfsTer2
ENST00000369244.6:c.1628dup ENSP00000358247.1:p.Asn543LysfsTer2
NM_001278716.1:c.1628dup NP_001265645.1:p.Asn543LysfsTer2
NM_012160.4:c.1628dup NP_036292.2:p.Asn543LysfsTer2
NR_103836.1:n.1673dup
XM_005266930.1:c.1556dup XP_005266987.1:p.Asn519LysfsTer2
XM_005266930.3:c.1556dup XP_005266987.1:p.Asn519LysfsTer2
XM_017010726.1:c.1628dup XP_016866215.1:p.Asn543LysfsTer2
XM_017010727.2:c.1556dup XP_016866216.1:p.Asn519LysfsTer2
XM_017010728.1:c.902dup XP_016866217.1:p.Asn301LysfsTer2
NM_001278716.2:c.1628dup MANE Select NP_001265645.1:p.Asn543LysfsTer2
NR_103836.2:n.1613dup
NM_012160.5:c.1628dup NP_036292.2:p.Asn543LysfsTer2