Canonical Allele Identifier: CA2634762484

Gene: FBXO31

Linked Data

• gnomAD v4: 16-87331055-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87331055C>A , CM000678.2:g.87331055C>A	GRCh38
NC_000016.9:g.87364661C>A , CM000678.1:g.87364661C>A	GRCh37
NC_000016.8:g.85922162C>A	NCBI36
NG_047196.1:g.66053G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636077.2:c.*233G>T	ENSP00000490402.2:n.*233G>T
ENST00000311635.12:c.*233G>T MANE Select	ENSP00000310841.4:n.*233G>T
ENST00000618298.6:c.*233G>T	ENSP00000479703.1:n.*233G>T
ENST00000311635.11:c.*233G>T	ENSP00000310841.4:n.*233G>T
ENST00000565593.1:c.*559G>T	ENSP00000455772.1:n.*559G>T
ENST00000568879.1:c.388+2831G>T
ENST00000618298.4:c.*233G>T	ENSP00000479703.1:n.*233G>T
NM_001282683.1:c.*233G>T	NP_001269612.1:n.*233G>T
NM_024735.4:c.*233G>T	NP_079011.3:n.*233G>T
NM_024735.5:c.*233G>T MANE Select	NP_079011.3:n.*233G>T
NM_001282683.2:c.*233G>T	NP_001269612.1:n.*233G>T