Canonical Allele Identifier: CA2163977725

Gene: CYFIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903618_22903620delinsCAG , CM000677.2:g.22903618_22903620delinsCAG	GRCh38
NC_000015.9:g.22969448_22969450delinsCTG , CM000677.1:g.22969448_22969450delinsCTG	GRCh37
NC_000015.8:g.20520889_20520891delinsCTG	NCBI36
NG_054889.1:g.82287_82289delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2582+86_2582+88delinsCTG	ENSP00000479802.2:n.2582+86_2582+88delinsCTG
ENST00000617928.5:c.2588+86_2588+88delinsCTG MANE Select	ENSP00000481038.1:n.2588+86_2588+88delinsCTG
ENST00000610365.4:c.2588+86_2588+88delinsCTG	ENSP00000478779.1:n.2588+86_2588+88delinsCTG
ENST00000617556.4:c.1295+86_1295+88delinsCTG	ENSP00000480525.1:n.1295+86_1295+88delinsCTG
ENST00000617928.4:c.2588+86_2588+88delinsCTG	ENSP00000481038.1:n.2588+86_2588+88delinsCTG
ENST00000619348.4:n.1735+86_1735+88delinsCTG
NM_001033028.1:c.1295+86_1295+88delinsCTG	NP_001028200.1:n.1295+86_1295+88delinsCTG
NM_001287810.1:c.2588+86_2588+88delinsCTG	NP_001274739.1:n.2588+86_2588+88delinsCTG
NM_014608.3:c.2588+86_2588+88delinsCTG	NP_055423.1:n.2588+86_2588+88delinsCTG
XM_011543873.1:c.2987+86_2987+88delinsCTG	XP_011542175.1:n.2987+86_2987+88delinsCTG
XM_011543874.1:c.2987+86_2987+88delinsCTG	XP_011542176.1:n.2987+86_2987+88delinsCTG
XM_011543875.1:c.2987+86_2987+88delinsCTG	XP_011542177.1:n.2987+86_2987+88delinsCTG
XM_011543876.1:c.2582+86_2582+88delinsCTG	XP_011542178.1:n.2582+86_2582+88delinsCTG
NM_001033028.2:c.1295+86_1295+88delinsCTG	NP_001028200.1:n.1295+86_1295+88delinsCTG
NM_001287810.3:c.2588+86_2588+88delinsCTG	NP_001274739.1:n.2588+86_2588+88delinsCTG
NM_001324119.2:c.2690+86_2690+88delinsCTG	NP_001311048.1:n.2690+86_2690+88delinsCTG
NM_001324120.2:c.2588+86_2588+88delinsCTG	NP_001311049.1:n.2588+86_2588+88delinsCTG
NM_001324122.2:c.908+86_908+88delinsCTG	NP_001311051.1:n.908+86_908+88delinsCTG
NM_001324123.2:c.2588+86_2588+88delinsCTG	NP_001311052.1:n.2588+86_2588+88delinsCTG
NM_001324124.2:c.2498+86_2498+88delinsCTG	NP_001311053.1:n.2498+86_2498+88delinsCTG
NM_001324125.2:c.2222+86_2222+88delinsCTG	NP_001311054.1:n.2222+86_2222+88delinsCTG
NM_001324126.2:c.2486+86_2486+88delinsCTG	NP_001311055.1:n.2486+86_2486+88delinsCTG
NM_014608.5:c.2588+86_2588+88delinsCTG	NP_055423.1:n.2588+86_2588+88delinsCTG
XM_011543873.3:c.2987+86_2987+88delinsCTG	XP_011542175.1:n.2987+86_2987+88delinsCTG
XM_011543874.2:c.2987+86_2987+88delinsCTG	XP_011542176.1:n.2987+86_2987+88delinsCTG
XM_011543876.3:c.2684+86_2684+88delinsCTG	XP_011542178.2:n.2684+86_2684+88delinsCTG
XM_017022023.2:c.3089+86_3089+88delinsCTG	XP_016877512.1:n.3089+86_3089+88delinsCTG
XM_017022024.2:c.2987+86_2987+88delinsCTG	XP_016877513.1:n.2987+86_2987+88delinsCTG
XM_024449876.1:c.2987+86_2987+88delinsCTG	XP_024305644.1:n.2987+86_2987+88delinsCTG
XM_024449877.1:c.2588+86_2588+88delinsCTG	XP_024305645.1:n.2588+86_2588+88delinsCTG
NM_014608.6:c.2588+86_2588+88delinsCTG MANE Select	NP_055423.1:n.2588+86_2588+88delinsCTG
NM_001287810.4:c.2588+86_2588+88delinsCTG	NP_001274739.1:n.2588+86_2588+88delinsCTG
NM_001324122.3:c.908+86_908+88delinsCTG	NP_001311051.1:n.908+86_908+88delinsCTG
NM_001324123.3:c.2588+86_2588+88delinsCTG	NP_001311052.1:n.2588+86_2588+88delinsCTG
NM_001324124.3:c.2498+86_2498+88delinsCTG	NP_001311053.1:n.2498+86_2498+88delinsCTG
NM_001324125.3:c.2222+86_2222+88delinsCTG	NP_001311054.1:n.2222+86_2222+88delinsCTG
NM_001324126.3:c.2486+86_2486+88delinsCTG	NP_001311055.1:n.2486+86_2486+88delinsCTG
NM_001033028.3:c.1295+86_1295+88delinsCTG	NP_001028200.1:n.1295+86_1295+88delinsCTG