Canonical Allele Identifier: CA2634762469
Gene: FBXO31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87331047G>A , CM000678.2:g.87331047G>A GRCh38
NC_000016.9:g.87364653G>A , CM000678.1:g.87364653G>A GRCh37
NC_000016.8:g.85922154G>A NCBI36
NG_047196.1:g.66061C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000636077.2:c.*241C>T ENSP00000490402.2:n.*241C>T
ENST00000311635.12:c.*241C>T MANE Select ENSP00000310841.4:n.*241C>T
ENST00000618298.6:c.*241C>T ENSP00000479703.1:n.*241C>T
ENST00000311635.11:c.*241C>T ENSP00000310841.4:n.*241C>T
ENST00000565593.1:c.*567C>T ENSP00000455772.1:n.*567C>T
ENST00000568879.1:c.388+2839C>T
ENST00000618298.4:c.*241C>T ENSP00000479703.1:n.*241C>T
NM_001282683.1:c.*241C>T NP_001269612.1:n.*241C>T
NM_024735.4:c.*241C>T NP_079011.3:n.*241C>T
NM_024735.5:c.*241C>T MANE Select NP_079011.3:n.*241C>T
NM_001282683.2:c.*241C>T NP_001269612.1:n.*241C>T