Canonical Allele Identifier: CA2163977936

Gene: CYFIP1

Linked Data

• dbSNP Id: rs2060477626

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903731_22903733del , CM000677.2:g.22903731_22903733del	GRCh38
NC_000015.9:g.22969338_22969340del , CM000677.1:g.22969338_22969340del	GRCh37
NC_000015.8:g.20520779_20520781del	NCBI36
NG_054889.1:g.82177_82179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2558_2560del	ENSP00000479802.2:p.Tyr853del
ENST00000617928.5:c.2564_2566del MANE Select	ENSP00000481038.1:p.Tyr855del
ENST00000610365.4:c.2564_2566del	ENSP00000478779.1:p.Tyr855del
ENST00000617556.4:c.1271_1273del	ENSP00000480525.1:p.Tyr424del
ENST00000617928.4:c.2564_2566del	ENSP00000481038.1:p.Tyr855del
ENST00000619348.4:n.1711_1713del
NM_001033028.1:c.1271_1273del	NP_001028200.1:p.Tyr424del
NM_001287810.1:c.2564_2566del	NP_001274739.1:p.Tyr855del
NM_014608.3:c.2564_2566del	NP_055423.1:p.Tyr855del
XM_011543873.1:c.2963_2965del	XP_011542175.1:p.Tyr988del
XM_011543874.1:c.2963_2965del	XP_011542176.1:p.Tyr988del
XM_011543875.1:c.2963_2965del	XP_011542177.1:p.Tyr988del
XM_011543876.1:c.2558_2560del	XP_011542178.1:p.Tyr853del
NM_001033028.2:c.1271_1273del	NP_001028200.1:p.Tyr424del
NM_001287810.3:c.2564_2566del	NP_001274739.1:p.Tyr855del
NM_001324119.2:c.2666_2668del	NP_001311048.1:p.Tyr889del
NM_001324120.2:c.2564_2566del	NP_001311049.1:p.Tyr855del
NM_001324122.2:c.884_886del	NP_001311051.1:p.Tyr295del
NM_001324123.2:c.2564_2566del	NP_001311052.1:p.Tyr855del
NM_001324124.2:c.2474_2476del	NP_001311053.1:p.Tyr825del
NM_001324125.2:c.2198_2200del	NP_001311054.1:p.Tyr733del
NM_001324126.2:c.2462_2464del	NP_001311055.1:p.Tyr821del
NM_014608.5:c.2564_2566del	NP_055423.1:p.Tyr855del
XM_011543873.3:c.2963_2965del	XP_011542175.1:p.Tyr988del
XM_011543874.2:c.2963_2965del	XP_011542176.1:p.Tyr988del
XM_011543876.3:c.2660_2662del	XP_011542178.2:p.Tyr887del
XM_017022023.2:c.3065_3067del	XP_016877512.1:p.Tyr1022del
XM_017022024.2:c.2963_2965del	XP_016877513.1:p.Tyr988del
XM_024449876.1:c.2963_2965del	XP_024305644.1:p.Tyr988del
XM_024449877.1:c.2564_2566del	XP_024305645.1:p.Tyr855del
NM_014608.6:c.2564_2566del MANE Select	NP_055423.1:p.Tyr855del
NM_001287810.4:c.2564_2566del	NP_001274739.1:p.Tyr855del
NM_001324122.3:c.884_886del	NP_001311051.1:p.Tyr295del
NM_001324123.3:c.2564_2566del	NP_001311052.1:p.Tyr855del
NM_001324124.3:c.2474_2476del	NP_001311053.1:p.Tyr825del
NM_001324125.3:c.2198_2200del	NP_001311054.1:p.Tyr733del
NM_001324126.3:c.2462_2464del	NP_001311055.1:p.Tyr821del
NM_001033028.3:c.1271_1273del	NP_001028200.1:p.Tyr424del