Canonical Allele Identifier: CA7425085

Gene: CYFIP1

Linked Data

• dbSNP Id: rs761267174
• ExAC: 15:22969151 T / TTGG
• gnomAD v2: 15-22969151-T-TTGG
• gnomAD v4: 15-22903911-G-GCAC
• MyVariant Identifiers: chr15:g.22969151_22969152insTGG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903914_22903916dup , CM000677.2:g.22903914_22903916dup	GRCh38
NC_000015.9:g.22969154_22969156dup , CM000677.1:g.22969154_22969156dup	GRCh37
NC_000015.8:g.20520595_20520597dup	NCBI36
NG_054889.1:g.81993_81995dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2383-9_2383-7dup	ENSP00000479802.2:n.2383-9_2383-7dup
ENST00000617928.5:c.2389-9_2389-7dup MANE Select	ENSP00000481038.1:n.2389-9_2389-7dup
ENST00000610365.4:c.2389-9_2389-7dup	ENSP00000478779.1:n.2389-9_2389-7dup
ENST00000617556.4:c.1096-9_1096-7dup	ENSP00000480525.1:n.1096-9_1096-7dup
ENST00000617928.4:c.2389-9_2389-7dup	ENSP00000481038.1:n.2389-9_2389-7dup
ENST00000619290.4:n.782-9_782-7dup
ENST00000619348.4:n.1527_1529dup
NM_001033028.1:c.1096-9_1096-7dup	NP_001028200.1:n.1096-9_1096-7dup
NM_001287810.1:c.2389-9_2389-7dup	NP_001274739.1:n.2389-9_2389-7dup
NM_014608.3:c.2389-9_2389-7dup	NP_055423.1:n.2389-9_2389-7dup
XM_011543873.1:c.2788-9_2788-7dup	XP_011542175.1:n.2788-9_2788-7dup
XM_011543874.1:c.2788-9_2788-7dup	XP_011542176.1:n.2788-9_2788-7dup
XM_011543875.1:c.2788-9_2788-7dup	XP_011542177.1:n.2788-9_2788-7dup
XM_011543876.1:c.2383-9_2383-7dup	XP_011542178.1:n.2383-9_2383-7dup
NM_001033028.2:c.1096-9_1096-7dup	NP_001028200.1:n.1096-9_1096-7dup
NM_001287810.3:c.2389-9_2389-7dup	NP_001274739.1:n.2389-9_2389-7dup
NM_001324119.2:c.2491-9_2491-7dup	NP_001311048.1:n.2491-9_2491-7dup
NM_001324120.2:c.2389-9_2389-7dup	NP_001311049.1:n.2389-9_2389-7dup
NM_001324122.2:c.709-9_709-7dup	NP_001311051.1:n.709-9_709-7dup
NM_001324123.2:c.2389-9_2389-7dup	NP_001311052.1:n.2389-9_2389-7dup
NM_001324124.2:c.2299-9_2299-7dup	NP_001311053.1:n.2299-9_2299-7dup
NM_001324125.2:c.2023-9_2023-7dup	NP_001311054.1:n.2023-9_2023-7dup
NM_001324126.2:c.2287-9_2287-7dup	NP_001311055.1:n.2287-9_2287-7dup
NM_014608.5:c.2389-9_2389-7dup	NP_055423.1:n.2389-9_2389-7dup
XM_011543873.3:c.2788-9_2788-7dup	XP_011542175.1:n.2788-9_2788-7dup
XM_011543874.2:c.2788-9_2788-7dup	XP_011542176.1:n.2788-9_2788-7dup
XM_011543876.3:c.2485-9_2485-7dup	XP_011542178.2:n.2485-9_2485-7dup
XM_017022023.2:c.2890-9_2890-7dup	XP_016877512.1:n.2890-9_2890-7dup
XM_017022024.2:c.2788-9_2788-7dup	XP_016877513.1:n.2788-9_2788-7dup
XM_024449876.1:c.2788-9_2788-7dup	XP_024305644.1:n.2788-9_2788-7dup
XM_024449877.1:c.2389-9_2389-7dup	XP_024305645.1:n.2389-9_2389-7dup
NM_014608.6:c.2389-9_2389-7dup MANE Select	NP_055423.1:n.2389-9_2389-7dup
NM_001287810.4:c.2389-9_2389-7dup	NP_001274739.1:n.2389-9_2389-7dup
NM_001324122.3:c.709-9_709-7dup	NP_001311051.1:n.709-9_709-7dup
NM_001324123.3:c.2389-9_2389-7dup	NP_001311052.1:n.2389-9_2389-7dup
NM_001324124.3:c.2299-9_2299-7dup	NP_001311053.1:n.2299-9_2299-7dup
NM_001324125.3:c.2023-9_2023-7dup	NP_001311054.1:n.2023-9_2023-7dup
NM_001324126.3:c.2287-9_2287-7dup	NP_001311055.1:n.2287-9_2287-7dup
NM_001033028.3:c.1096-9_1096-7dup	NP_001028200.1:n.1096-9_1096-7dup