Canonical Allele Identifier: CA806217759

Gene: FBXL7

Linked Data

• dbSNP Id: rs1353283026
• MyVariant Identifiers: chr5:g.15783497_15783498insA (hg19) ; chr5:g.15783388_15783389insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783394dup , CM000667.2:g.15783394dup	GRCh38
NC_000005.9:g.15783503dup , CM000667.1:g.15783503dup	GRCh37
NC_000005.8:g.15836503dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504595.2:c.128-144496dup MANE Select	ENSP00000423630.1:n.128-144496dup
ENST00000504595.1:c.128-144496dup	ENSP00000423630.1:n.128-144496dup
ENST00000510662.1:c.-14-144496dup	ENSP00000425184.1:n.-14-144496dup
NM_001278317.1:c.-14-144496dup	NP_001265246.1:n.-14-144496dup
NM_012304.4:c.128-144496dup	NP_036436.1:n.128-144496dup
XM_005248273.3:c.113-144496dup	XP_005248330.1:n.113-144496dup
XM_011513998.1:c.-91-51383dup	XP_011512300.1:n.-91-51383dup
XM_017009262.2:c.113-144496dup	XP_016864751.1:n.113-144496dup
NM_012304.5:c.128-144496dup MANE Select	NP_036436.1:n.128-144496dup
NM_001278317.2:c.-14-144496dup	NP_001265246.1:n.-14-144496dup