Canonical Allele Identifier: CA806217798

Gene: FBXL7

Linked Data

• dbSNP Id: rs1276053363
• MyVariant Identifiers: chr5:g.15783565T>C (hg19) ; chr5:g.15783456T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783456T>C , CM000667.2:g.15783456T>C	GRCh38
NC_000005.9:g.15783565T>C , CM000667.1:g.15783565T>C	GRCh37
NC_000005.8:g.15836565T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144434T>C MANE Select	ENSP00000423630.1:n.128-144434T>C
ENST00000504595.1:c.128-144434T>C	ENSP00000423630.1:n.128-144434T>C
ENST00000510662.1:c.-14-144434T>C	ENSP00000425184.1:n.-14-144434T>C
NM_001278317.1:c.-14-144434T>C	NP_001265246.1:n.-14-144434T>C
NM_012304.4:c.128-144434T>C	NP_036436.1:n.128-144434T>C
XM_005248273.3:c.113-144434T>C	XP_005248330.1:n.113-144434T>C
XM_011513998.1:c.-91-51321T>C	XP_011512300.1:n.-91-51321T>C
XM_017009262.2:c.113-144434T>C	XP_016864751.1:n.113-144434T>C
NM_012304.5:c.128-144434T>C MANE Select	NP_036436.1:n.128-144434T>C
NM_001278317.2:c.-14-144434T>C	NP_001265246.1:n.-14-144434T>C