Canonical Allele Identifier: CA451573320

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99374571T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926695T>A , CM000668.2:g.98926695T>A	GRCh38
NC_000006.11:g.99374571T>A , CM000668.1:g.99374571T>A	GRCh37
NC_000006.10:g.99481292T>A	NCBI36
NG_033903.1:g.26312A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.294A>T MANE Select	ENSP00000358247.1:p.Arg98=
ENST00000229971.2:c.294A>T	ENSP00000229971.1:p.Arg98=
ENST00000369244.6:c.294A>T	ENSP00000358247.1:p.Arg98=
NM_001278716.1:c.294A>T	NP_001265645.1:p.Arg98=
NM_012160.4:c.294A>T	NP_036292.2:p.Arg98=
NR_103836.1:n.685A>T
NR_103837.1:n.685A>T
XM_005266930.1:c.294A>T	XP_005266987.1:p.Arg98=
XM_011535748.1:c.294A>T	XP_011534050.1:p.Arg98=
XM_005266930.3:c.294A>T	XP_005266987.1:p.Arg98=
XM_011535748.3:c.294A>T	XP_011534050.1:p.Arg98=
XM_017010726.1:c.294A>T	XP_016866215.1:p.Arg98=
XM_017010727.2:c.294A>T	XP_016866216.1:p.Arg98=
XM_017010728.1:c.-509A>T	XP_016866217.1:n.-509A>T
NM_001278716.2:c.294A>T MANE Select	NP_001265645.1:p.Arg98=
NR_103836.2:n.625A>T
NR_103837.2:n.625A>T
NM_012160.5:c.294A>T	NP_036292.2:p.Arg98=