Canonical Allele Identifier: CA11921614

Gene: FBXL7

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15674526G>A , CM000667.2:g.15674526G>A	GRCh38
NC_000005.9:g.15674635G>A , CM000667.1:g.15674635G>A	GRCh37
NC_000005.8:g.15727635G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.127+58454G>A MANE Select	ENSP00000423630.1:n.127+58454G>A
ENST00000504595.1:c.127+58454G>A	ENSP00000423630.1:n.127+58454G>A
ENST00000510662.1:c.-15+58454G>A	ENSP00000425184.1:n.-15+58454G>A
NM_001278317.1:c.-15+58454G>A	NP_001265246.1:n.-15+58454G>A
NM_012304.4:c.127+58454G>A	NP_036436.1:n.127+58454G>A
XM_005248273.3:c.112+58454G>A	XP_005248330.1:n.112+58454G>A
XM_011513998.1:c.-92+58454G>A	XP_011512300.1:n.-92+58454G>A
XM_017009262.2:c.112+58454G>A	XP_016864751.1:n.112+58454G>A
NM_012304.5:c.127+58454G>A MANE Select	NP_036436.1:n.127+58454G>A
NM_001278317.2:c.-15+58454G>A	NP_001265246.1:n.-15+58454G>A