Canonical Allele Identifier: CA2163977838

Gene: CYFIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903685_22903687delinsCTG , CM000677.2:g.22903685_22903687delinsCTG	GRCh38
NC_000015.9:g.22969381_22969383delinsCAG , CM000677.1:g.22969381_22969383delinsCAG	GRCh37
NC_000015.8:g.20520822_20520824delinsCAG	NCBI36
NG_054889.1:g.82220_82222delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2582+19_2582+21delinsCAG	ENSP00000479802.2:n.2582+19_2582+21delinsCAG
ENST00000617928.5:c.2588+19_2588+21delinsCAG MANE Select	ENSP00000481038.1:n.2588+19_2588+21delinsCAG
ENST00000610365.4:c.2588+19_2588+21delinsCAG	ENSP00000478779.1:n.2588+19_2588+21delinsCAG
ENST00000617556.4:c.1295+19_1295+21delinsCAG	ENSP00000480525.1:n.1295+19_1295+21delinsCAG
ENST00000617928.4:c.2588+19_2588+21delinsCAG	ENSP00000481038.1:n.2588+19_2588+21delinsCAG
ENST00000619348.4:n.1735+19_1735+21delinsCAG
NM_001033028.1:c.1295+19_1295+21delinsCAG	NP_001028200.1:n.1295+19_1295+21delinsCAG
NM_001287810.1:c.2588+19_2588+21delinsCAG	NP_001274739.1:n.2588+19_2588+21delinsCAG
NM_014608.3:c.2588+19_2588+21delinsCAG	NP_055423.1:n.2588+19_2588+21delinsCAG
XM_011543873.1:c.2987+19_2987+21delinsCAG	XP_011542175.1:n.2987+19_2987+21delinsCAG
XM_011543874.1:c.2987+19_2987+21delinsCAG	XP_011542176.1:n.2987+19_2987+21delinsCAG
XM_011543875.1:c.2987+19_2987+21delinsCAG	XP_011542177.1:n.2987+19_2987+21delinsCAG
XM_011543876.1:c.2582+19_2582+21delinsCAG	XP_011542178.1:n.2582+19_2582+21delinsCAG
NM_001033028.2:c.1295+19_1295+21delinsCAG	NP_001028200.1:n.1295+19_1295+21delinsCAG
NM_001287810.3:c.2588+19_2588+21delinsCAG	NP_001274739.1:n.2588+19_2588+21delinsCAG
NM_001324119.2:c.2690+19_2690+21delinsCAG	NP_001311048.1:n.2690+19_2690+21delinsCAG
NM_001324120.2:c.2588+19_2588+21delinsCAG	NP_001311049.1:n.2588+19_2588+21delinsCAG
NM_001324122.2:c.908+19_908+21delinsCAG	NP_001311051.1:n.908+19_908+21delinsCAG
NM_001324123.2:c.2588+19_2588+21delinsCAG	NP_001311052.1:n.2588+19_2588+21delinsCAG
NM_001324124.2:c.2498+19_2498+21delinsCAG	NP_001311053.1:n.2498+19_2498+21delinsCAG
NM_001324125.2:c.2222+19_2222+21delinsCAG	NP_001311054.1:n.2222+19_2222+21delinsCAG
NM_001324126.2:c.2486+19_2486+21delinsCAG	NP_001311055.1:n.2486+19_2486+21delinsCAG
NM_014608.5:c.2588+19_2588+21delinsCAG	NP_055423.1:n.2588+19_2588+21delinsCAG
XM_011543873.3:c.2987+19_2987+21delinsCAG	XP_011542175.1:n.2987+19_2987+21delinsCAG
XM_011543874.2:c.2987+19_2987+21delinsCAG	XP_011542176.1:n.2987+19_2987+21delinsCAG
XM_011543876.3:c.2684+19_2684+21delinsCAG	XP_011542178.2:n.2684+19_2684+21delinsCAG
XM_017022023.2:c.3089+19_3089+21delinsCAG	XP_016877512.1:n.3089+19_3089+21delinsCAG
XM_017022024.2:c.2987+19_2987+21delinsCAG	XP_016877513.1:n.2987+19_2987+21delinsCAG
XM_024449876.1:c.2987+19_2987+21delinsCAG	XP_024305644.1:n.2987+19_2987+21delinsCAG
XM_024449877.1:c.2588+19_2588+21delinsCAG	XP_024305645.1:n.2588+19_2588+21delinsCAG
NM_014608.6:c.2588+19_2588+21delinsCAG MANE Select	NP_055423.1:n.2588+19_2588+21delinsCAG
NM_001287810.4:c.2588+19_2588+21delinsCAG	NP_001274739.1:n.2588+19_2588+21delinsCAG
NM_001324122.3:c.908+19_908+21delinsCAG	NP_001311051.1:n.908+19_908+21delinsCAG
NM_001324123.3:c.2588+19_2588+21delinsCAG	NP_001311052.1:n.2588+19_2588+21delinsCAG
NM_001324124.3:c.2498+19_2498+21delinsCAG	NP_001311053.1:n.2498+19_2498+21delinsCAG
NM_001324125.3:c.2222+19_2222+21delinsCAG	NP_001311054.1:n.2222+19_2222+21delinsCAG
NM_001324126.3:c.2486+19_2486+21delinsCAG	NP_001311055.1:n.2486+19_2486+21delinsCAG
NM_001033028.3:c.1295+19_1295+21delinsCAG	NP_001028200.1:n.1295+19_1295+21delinsCAG