Canonical Allele Identifier: CA2679757631

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875122-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875122G>A , CM000668.2:g.98875122G>A	GRCh38
NC_000006.11:g.99322998G>A , CM000668.1:g.99322998G>A	GRCh37
NC_000006.10:g.99429719G>A	NCBI36
NG_033903.1:g.77885C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+293C>T MANE Select	ENSP00000358247.1:n.1702+293C>T
ENST00000229971.2:c.1702+293C>T	ENSP00000229971.1:n.1702+293C>T
ENST00000369244.6:c.1702+293C>T	ENSP00000358247.1:n.1702+293C>T
NM_001278716.1:c.1702+293C>T	NP_001265645.1:n.1702+293C>T
NM_012160.4:c.1702+293C>T	NP_036292.2:n.1702+293C>T
NR_103836.1:n.1747+293C>T
XM_005266930.1:c.1630+293C>T	XP_005266987.1:n.1630+293C>T
XM_005266930.3:c.1630+293C>T	XP_005266987.1:n.1630+293C>T
XM_017010726.1:c.1702+293C>T	XP_016866215.1:n.1702+293C>T
XM_017010727.2:c.1630+293C>T	XP_016866216.1:n.1630+293C>T
XM_017010728.1:c.976+293C>T	XP_016866217.1:n.976+293C>T
NM_001278716.2:c.1702+293C>T MANE Select	NP_001265645.1:n.1702+293C>T
NR_103836.2:n.1687+293C>T
NM_012160.5:c.1702+293C>T	NP_036292.2:n.1702+293C>T