Canonical Allele Identifier: CA1649861562

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874461_98874462delinsCA , CM000668.2:g.98874461_98874462delinsCA	GRCh38
NC_000006.11:g.99322337_99322338delinsCA , CM000668.1:g.99322337_99322338delinsCA	GRCh37
NC_000006.10:g.99429058_99429059delinsCA	NCBI36
NG_033903.1:g.78545_78546delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1703-21_1703-20delinsTG MANE Select	ENSP00000358247.1:n.1703-21_1703-20delinsTG
ENST00000229971.2:c.1703-21_1703-20delinsTG	ENSP00000229971.1:n.1703-21_1703-20delinsTG
ENST00000369244.6:c.1703-21_1703-20delinsTG	ENSP00000358247.1:n.1703-21_1703-20delinsTG
NM_001278716.1:c.1703-21_1703-20delinsTG	NP_001265645.1:n.1703-21_1703-20delinsTG
NM_012160.4:c.1703-21_1703-20delinsTG	NP_036292.2:n.1703-21_1703-20delinsTG
NR_103836.1:n.1748-21_1748-20delinsTG
XM_005266930.1:c.1631-21_1631-20delinsTG	XP_005266987.1:n.1631-21_1631-20delinsTG
XM_005266930.3:c.1631-21_1631-20delinsTG	XP_005266987.1:n.1631-21_1631-20delinsTG
XM_017010726.1:c.1703-21_1703-20delinsTG	XP_016866215.1:n.1703-21_1703-20delinsTG
XM_017010727.2:c.1631-21_1631-20delinsTG	XP_016866216.1:n.1631-21_1631-20delinsTG
XM_017010728.1:c.977-21_977-20delinsTG	XP_016866217.1:n.977-21_977-20delinsTG
NM_001278716.2:c.1703-21_1703-20delinsTG MANE Select	NP_001265645.1:n.1703-21_1703-20delinsTG
NR_103836.2:n.1688-21_1688-20delinsTG
NM_012160.5:c.1703-21_1703-20delinsTG	NP_036292.2:n.1703-21_1703-20delinsTG