Canonical Allele Identifier: CA451573142

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99374439A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926563A>T , CM000668.2:g.98926563A>T	GRCh38
NC_000006.11:g.99374439A>T , CM000668.1:g.99374439A>T	GRCh37
NC_000006.10:g.99481160A>T	NCBI36
NG_033903.1:g.26444T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.426T>A MANE Select	ENSP00000358247.1:p.Val142=
ENST00000229971.2:c.426T>A	ENSP00000229971.1:p.Val142=
ENST00000369244.6:c.426T>A	ENSP00000358247.1:p.Val142=
NM_001278716.1:c.426T>A	NP_001265645.1:p.Val142=
NM_012160.4:c.426T>A	NP_036292.2:p.Val142=
NR_103836.1:n.817T>A
NR_103837.1:n.817T>A
XM_005266930.1:c.426T>A	XP_005266987.1:p.Val142=
XM_011535748.1:c.426T>A	XP_011534050.1:p.Val142=
XM_005266930.3:c.426T>A	XP_005266987.1:p.Val142=
XM_011535748.3:c.426T>A	XP_011534050.1:p.Val142=
XM_017010726.1:c.426T>A	XP_016866215.1:p.Val142=
XM_017010727.2:c.426T>A	XP_016866216.1:p.Val142=
XM_017010728.1:c.-377T>A	XP_016866217.1:n.-377T>A
NM_001278716.2:c.426T>A MANE Select	NP_001265645.1:p.Val142=
NR_103836.2:n.757T>A
NR_103837.2:n.757T>A
NM_012160.5:c.426T>A	NP_036292.2:p.Val142=