Canonical Allele Identifier: CA2679757568

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98874518-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874518_98874519insT , CM000668.2:g.98874518_98874519insT	GRCh38
NC_000006.11:g.99322394_99322395insT , CM000668.1:g.99322394_99322395insT	GRCh37
NC_000006.10:g.99429115_99429116insT	NCBI36
NG_033903.1:g.78488_78489insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1703-78_1703-77insA MANE Select	ENSP00000358247.1:n.1703-78_1703-77insA
ENST00000229971.2:c.1703-78_1703-77insA	ENSP00000229971.1:n.1703-78_1703-77insA
ENST00000369244.6:c.1703-78_1703-77insA	ENSP00000358247.1:n.1703-78_1703-77insA
NM_001278716.1:c.1703-78_1703-77insA	NP_001265645.1:n.1703-78_1703-77insA
NM_012160.4:c.1703-78_1703-77insA	NP_036292.2:n.1703-78_1703-77insA
NR_103836.1:n.1748-78_1748-77insA
XM_005266930.1:c.1631-78_1631-77insA	XP_005266987.1:n.1631-78_1631-77insA
XM_005266930.3:c.1631-78_1631-77insA	XP_005266987.1:n.1631-78_1631-77insA
XM_017010726.1:c.1703-78_1703-77insA	XP_016866215.1:n.1703-78_1703-77insA
XM_017010727.2:c.1631-78_1631-77insA	XP_016866216.1:n.1631-78_1631-77insA
XM_017010728.1:c.977-78_977-77insA	XP_016866217.1:n.977-78_977-77insA
NM_001278716.2:c.1703-78_1703-77insA MANE Select	NP_001265645.1:n.1703-78_1703-77insA
NR_103836.2:n.1688-78_1688-77insA
NM_012160.5:c.1703-78_1703-77insA	NP_036292.2:n.1703-78_1703-77insA