Canonical Allele Identifier: CA391334883

Gene: CYFIP1

Linked Data

• MyVariant Identifiers: chr15:g.22969170A>T (hg19) ; chr15:g.22903898T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903898T>A , CM000677.2:g.22903898T>A	GRCh38
NC_000015.9:g.22969170A>T , CM000677.1:g.22969170A>T	GRCh37
NC_000015.8:g.20520611A>T	NCBI36
NG_054889.1:g.82009A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2390A>T	ENSP00000479802.2:p.Asp797Val
ENST00000617928.5:c.2396A>T MANE Select	ENSP00000481038.1:p.Asp799Val
ENST00000610365.4:c.2396A>T	ENSP00000478779.1:p.Asp799Val
ENST00000617556.4:c.1103A>T	ENSP00000480525.1:p.Asp368Val
ENST00000617928.4:c.2396A>T	ENSP00000481038.1:p.Asp799Val
ENST00000619290.4:n.789A>T
ENST00000619348.4:n.1543A>T
NM_001033028.1:c.1103A>T	NP_001028200.1:p.Asp368Val
NM_001287810.1:c.2396A>T	NP_001274739.1:p.Asp799Val
NM_014608.3:c.2396A>T	NP_055423.1:p.Asp799Val
XM_011543873.1:c.2795A>T	XP_011542175.1:p.Asp932Val
XM_011543874.1:c.2795A>T	XP_011542176.1:p.Asp932Val
XM_011543875.1:c.2795A>T	XP_011542177.1:p.Asp932Val
XM_011543876.1:c.2390A>T	XP_011542178.1:p.Asp797Val
NM_001033028.2:c.1103A>T	NP_001028200.1:p.Asp368Val
NM_001287810.3:c.2396A>T	NP_001274739.1:p.Asp799Val
NM_001324119.2:c.2498A>T	NP_001311048.1:p.Asp833Val
NM_001324120.2:c.2396A>T	NP_001311049.1:p.Asp799Val
NM_001324122.2:c.716A>T	NP_001311051.1:p.Asp239Val
NM_001324123.2:c.2396A>T	NP_001311052.1:p.Asp799Val
NM_001324124.2:c.2306A>T	NP_001311053.1:p.Asp769Val
NM_001324125.2:c.2030A>T	NP_001311054.1:p.Asp677Val
NM_001324126.2:c.2294A>T	NP_001311055.1:p.Asp765Val
NM_014608.5:c.2396A>T	NP_055423.1:p.Asp799Val
XM_011543873.3:c.2795A>T	XP_011542175.1:p.Asp932Val
XM_011543874.2:c.2795A>T	XP_011542176.1:p.Asp932Val
XM_011543876.3:c.2492A>T	XP_011542178.2:p.Asp831Val
XM_017022023.2:c.2897A>T	XP_016877512.1:p.Asp966Val
XM_017022024.2:c.2795A>T	XP_016877513.1:p.Asp932Val
XM_024449876.1:c.2795A>T	XP_024305644.1:p.Asp932Val
XM_024449877.1:c.2396A>T	XP_024305645.1:p.Asp799Val
NM_014608.6:c.2396A>T MANE Select	NP_055423.1:p.Asp799Val
NM_001287810.4:c.2396A>T	NP_001274739.1:p.Asp799Val
NM_001324122.3:c.716A>T	NP_001311051.1:p.Asp239Val
NM_001324123.3:c.2396A>T	NP_001311052.1:p.Asp799Val
NM_001324124.3:c.2306A>T	NP_001311053.1:p.Asp769Val
NM_001324125.3:c.2030A>T	NP_001311054.1:p.Asp677Val
NM_001324126.3:c.2294A>T	NP_001311055.1:p.Asp765Val
NM_001033028.3:c.1103A>T	NP_001028200.1:p.Asp368Val