Canonical Allele Identifier: CA114898697

Gene: FBXL7

Linked Data

• dbSNP Id: rs59295191
• gnomAD v2: 5-15783450-A-C
• gnomAD v3: 5-15783341-A-C
• gnomAD v4: 5-15783341-A-C
• MyVariant Identifiers: chr5:g.15783450A>C (hg19) ; chr5:g.15783341A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783341A>C , CM000667.2:g.15783341A>C	GRCh38
NC_000005.9:g.15783450A>C , CM000667.1:g.15783450A>C	GRCh37
NC_000005.8:g.15836450A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144549A>C MANE Select	ENSP00000423630.1:n.128-144549A>C
ENST00000504595.1:c.128-144549A>C	ENSP00000423630.1:n.128-144549A>C
ENST00000510662.1:c.-14-144549A>C	ENSP00000425184.1:n.-14-144549A>C
NM_001278317.1:c.-14-144549A>C	NP_001265246.1:n.-14-144549A>C
NM_012304.4:c.128-144549A>C	NP_036436.1:n.128-144549A>C
XM_005248273.3:c.113-144549A>C	XP_005248330.1:n.113-144549A>C
XM_011513998.1:c.-91-51436A>C	XP_011512300.1:n.-91-51436A>C
XM_017009262.2:c.113-144549A>C	XP_016864751.1:n.113-144549A>C
NM_012304.5:c.128-144549A>C MANE Select	NP_036436.1:n.128-144549A>C
NM_001278317.2:c.-14-144549A>C	NP_001265246.1:n.-14-144549A>C