Canonical Allele Identifier: CA451573735

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99374706C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926830C>T , CM000668.2:g.98926830C>T	GRCh38
NC_000006.11:g.99374706C>T , CM000668.1:g.99374706C>T	GRCh37
NC_000006.10:g.99481427C>T	NCBI36
NG_033903.1:g.26177G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369244.7:c.159G>A MANE Select	ENSP00000358247.1:p.Gln53=
ENST00000229971.2:c.159G>A	ENSP00000229971.1:p.Gln53=
ENST00000369244.6:c.159G>A	ENSP00000358247.1:p.Gln53=
NM_001278716.1:c.159G>A	NP_001265645.1:p.Gln53=
NM_012160.4:c.159G>A	NP_036292.2:p.Gln53=
NR_103836.1:n.550G>A
NR_103837.1:n.550G>A
XM_005266930.1:c.159G>A	XP_005266987.1:p.Gln53=
XM_011535748.1:c.159G>A	XP_011534050.1:p.Gln53=
XM_005266930.3:c.159G>A	XP_005266987.1:p.Gln53=
XM_011535748.3:c.159G>A	XP_011534050.1:p.Gln53=
XM_017010726.1:c.159G>A	XP_016866215.1:p.Gln53=
XM_017010727.2:c.159G>A	XP_016866216.1:p.Gln53=
XM_017010728.1:c.-644G>A	XP_016866217.1:n.-644G>A
NM_001278716.2:c.159G>A MANE Select	NP_001265645.1:p.Gln53=
NR_103836.2:n.490G>A
NR_103837.2:n.490G>A
NM_012160.5:c.159G>A	NP_036292.2:p.Gln53=