Canonical Allele Identifier: CA451573340

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99374598A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926722A>C , CM000668.2:g.98926722A>C	GRCh38
NC_000006.11:g.99374598A>C , CM000668.1:g.99374598A>C	GRCh37
NC_000006.10:g.99481319A>C	NCBI36
NG_033903.1:g.26285T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.267T>G MANE Select	ENSP00000358247.1:p.Gly89=
ENST00000229971.2:c.267T>G	ENSP00000229971.1:p.Gly89=
ENST00000369244.6:c.267T>G	ENSP00000358247.1:p.Gly89=
NM_001278716.1:c.267T>G	NP_001265645.1:p.Gly89=
NM_012160.4:c.267T>G	NP_036292.2:p.Gly89=
NR_103836.1:n.658T>G
NR_103837.1:n.658T>G
XM_005266930.1:c.267T>G	XP_005266987.1:p.Gly89=
XM_011535748.1:c.267T>G	XP_011534050.1:p.Gly89=
XM_005266930.3:c.267T>G	XP_005266987.1:p.Gly89=
XM_011535748.3:c.267T>G	XP_011534050.1:p.Gly89=
XM_017010726.1:c.267T>G	XP_016866215.1:p.Gly89=
XM_017010727.2:c.267T>G	XP_016866216.1:p.Gly89=
XM_017010728.1:c.-536T>G	XP_016866217.1:n.-536T>G
NM_001278716.2:c.267T>G MANE Select	NP_001265645.1:p.Gly89=
NR_103836.2:n.598T>G
NR_103837.2:n.598T>G
NM_012160.5:c.267T>G	NP_036292.2:p.Gly89=