Canonical Allele Identifier: CA3933330
Community Standard Title: NM_001278716.2(FBXL4):c.*9A>G
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98874269T>C , CM000668.2:g.98874269T>C GRCh38
NC_000006.11:g.99322145T>C , CM000668.1:g.99322145T>C GRCh37
NC_000006.10:g.99428866T>C NCBI36
NG_033903.1:g.78738A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001278716.2:c.*9A>G MANE Select NP_001265645.1:n.*9A>G
ENST00000369244.7:c.*9A>G MANE Select ENSP00000358247.1:n.*9A>G
NM_001278716.1:c.*9A>G NP_001265645.1:n.*9A>G
NM_012160.4:c.*9A>G NP_036292.2:n.*9A>G
NM_012160.5:c.*9A>G NP_036292.2:n.*9A>G
NR_103836.1:n.1920A>G
NR_103836.2:n.1860A>G
ENST00000229971.2:c.*9A>G ENSP00000229971.1:n.*9A>G
ENST00000369244.6:c.*9A>G ENSP00000358247.1:n.*9A>G
XM_005266930.1:c.*9A>G XP_005266987.1:n.*9A>G
XM_005266930.3:c.*9A>G XP_005266987.1:n.*9A>G
XM_017010726.1:c.*9A>G XP_016866215.1:n.*9A>G
XM_017010727.2:c.*9A>G XP_016866216.1:n.*9A>G
XM_017010728.1:c.*9A>G XP_016866217.1:n.*9A>G