Canonical Allele Identifier: CA391334651

Gene: CYFIP1

Linked Data

• dbSNP Id: rs2142014895
• MyVariant Identifiers: chr15:g.22969230A>T (hg19) ; chr15:g.22903838T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903838T>A , CM000677.2:g.22903838T>A	GRCh38
NC_000015.9:g.22969230A>T , CM000677.1:g.22969230A>T	GRCh37
NC_000015.8:g.20520671A>T	NCBI36
NG_054889.1:g.82069A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2450A>T	ENSP00000479802.2:p.Asp817Val
ENST00000617928.5:c.2456A>T MANE Select	ENSP00000481038.1:p.Asp819Val
ENST00000610365.4:c.2456A>T	ENSP00000478779.1:p.Asp819Val
ENST00000617556.4:c.1163A>T	ENSP00000480525.1:p.Asp388Val
ENST00000617928.4:c.2456A>T	ENSP00000481038.1:p.Asp819Val
ENST00000619290.4:n.849A>T
ENST00000619348.4:n.1603A>T
NM_001033028.1:c.1163A>T	NP_001028200.1:p.Asp388Val
NM_001287810.1:c.2456A>T	NP_001274739.1:p.Asp819Val
NM_014608.3:c.2456A>T	NP_055423.1:p.Asp819Val
XM_011543873.1:c.2855A>T	XP_011542175.1:p.Asp952Val
XM_011543874.1:c.2855A>T	XP_011542176.1:p.Asp952Val
XM_011543875.1:c.2855A>T	XP_011542177.1:p.Asp952Val
XM_011543876.1:c.2450A>T	XP_011542178.1:p.Asp817Val
NM_001033028.2:c.1163A>T	NP_001028200.1:p.Asp388Val
NM_001287810.3:c.2456A>T	NP_001274739.1:p.Asp819Val
NM_001324119.2:c.2558A>T	NP_001311048.1:p.Asp853Val
NM_001324120.2:c.2456A>T	NP_001311049.1:p.Asp819Val
NM_001324122.2:c.776A>T	NP_001311051.1:p.Asp259Val
NM_001324123.2:c.2456A>T	NP_001311052.1:p.Asp819Val
NM_001324124.2:c.2366A>T	NP_001311053.1:p.Asp789Val
NM_001324125.2:c.2090A>T	NP_001311054.1:p.Asp697Val
NM_001324126.2:c.2354A>T	NP_001311055.1:p.Asp785Val
NM_014608.5:c.2456A>T	NP_055423.1:p.Asp819Val
XM_011543873.3:c.2855A>T	XP_011542175.1:p.Asp952Val
XM_011543874.2:c.2855A>T	XP_011542176.1:p.Asp952Val
XM_011543876.3:c.2552A>T	XP_011542178.2:p.Asp851Val
XM_017022023.2:c.2957A>T	XP_016877512.1:p.Asp986Val
XM_017022024.2:c.2855A>T	XP_016877513.1:p.Asp952Val
XM_024449876.1:c.2855A>T	XP_024305644.1:p.Asp952Val
XM_024449877.1:c.2456A>T	XP_024305645.1:p.Asp819Val
NM_014608.6:c.2456A>T MANE Select	NP_055423.1:p.Asp819Val
NM_001287810.4:c.2456A>T	NP_001274739.1:p.Asp819Val
NM_001324122.3:c.776A>T	NP_001311051.1:p.Asp259Val
NM_001324123.3:c.2456A>T	NP_001311052.1:p.Asp819Val
NM_001324124.3:c.2366A>T	NP_001311053.1:p.Asp789Val
NM_001324125.3:c.2090A>T	NP_001311054.1:p.Asp697Val
NM_001324126.3:c.2354A>T	NP_001311055.1:p.Asp785Val
NM_001033028.3:c.1163A>T	NP_001028200.1:p.Asp388Val