Canonical Allele Identifier: CA451573168

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99374451T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926575T>G , CM000668.2:g.98926575T>G	GRCh38
NC_000006.11:g.99374451T>G , CM000668.1:g.99374451T>G	GRCh37
NC_000006.10:g.99481172T>G	NCBI36
NG_033903.1:g.26432A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.414A>C MANE Select	ENSP00000358247.1:p.Thr138=
ENST00000229971.2:c.414A>C	ENSP00000229971.1:p.Thr138=
ENST00000369244.6:c.414A>C	ENSP00000358247.1:p.Thr138=
NM_001278716.1:c.414A>C	NP_001265645.1:p.Thr138=
NM_012160.4:c.414A>C	NP_036292.2:p.Thr138=
NR_103836.1:n.805A>C
NR_103837.1:n.805A>C
XM_005266930.1:c.414A>C	XP_005266987.1:p.Thr138=
XM_011535748.1:c.414A>C	XP_011534050.1:p.Thr138=
XM_005266930.3:c.414A>C	XP_005266987.1:p.Thr138=
XM_011535748.3:c.414A>C	XP_011534050.1:p.Thr138=
XM_017010726.1:c.414A>C	XP_016866215.1:p.Thr138=
XM_017010727.2:c.414A>C	XP_016866216.1:p.Thr138=
XM_017010728.1:c.-389A>C	XP_016866217.1:n.-389A>C
NM_001278716.2:c.414A>C MANE Select	NP_001265645.1:p.Thr138=
NR_103836.2:n.745A>C
NR_103837.2:n.745A>C
NM_012160.5:c.414A>C	NP_036292.2:p.Thr138=