Canonical Allele Identifier: CA114898722

Gene: FBXL7

Linked Data

• dbSNP Id: rs774275617
• MyVariant Identifiers: chr5:g.15783647_15783648insA (hg19) ; chr5:g.15783538_15783539insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783541dup , CM000667.2:g.15783541dup	GRCh38
NC_000005.9:g.15783650dup , CM000667.1:g.15783650dup	GRCh37
NC_000005.8:g.15836650dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144349dup MANE Select	ENSP00000423630.1:n.128-144349dup
ENST00000504595.1:c.128-144349dup	ENSP00000423630.1:n.128-144349dup
ENST00000510662.1:c.-14-144349dup	ENSP00000425184.1:n.-14-144349dup
NM_001278317.1:c.-14-144349dup	NP_001265246.1:n.-14-144349dup
NM_012304.4:c.128-144349dup	NP_036436.1:n.128-144349dup
XM_005248273.3:c.113-144349dup	XP_005248330.1:n.113-144349dup
XM_011513998.1:c.-91-51236dup	XP_011512300.1:n.-91-51236dup
XM_017009262.2:c.113-144349dup	XP_016864751.1:n.113-144349dup
NM_012304.5:c.128-144349dup MANE Select	NP_036436.1:n.128-144349dup
NM_001278317.2:c.-14-144349dup	NP_001265246.1:n.-14-144349dup