Canonical Allele Identifier: CA391334544

Gene: CYFIP1

Linked Data

• MyVariant Identifiers: chr15:g.22969257C>T (hg19) ; chr15:g.22903811G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903811G>A , CM000677.2:g.22903811G>A	GRCh38
NC_000015.9:g.22969257C>T , CM000677.1:g.22969257C>T	GRCh37
NC_000015.8:g.20520698C>T	NCBI36
NG_054889.1:g.82096C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2477C>T	ENSP00000479802.2:p.Ala826Val
ENST00000617928.5:c.2483C>T MANE Select	ENSP00000481038.1:p.Ala828Val
ENST00000610365.4:c.2483C>T	ENSP00000478779.1:p.Ala828Val
ENST00000617556.4:c.1190C>T	ENSP00000480525.1:p.Ala397Val
ENST00000617928.4:c.2483C>T	ENSP00000481038.1:p.Ala828Val
ENST00000619290.4:n.876C>T
ENST00000619348.4:n.1630C>T
NM_001033028.1:c.1190C>T	NP_001028200.1:p.Ala397Val
NM_001287810.1:c.2483C>T	NP_001274739.1:p.Ala828Val
NM_014608.3:c.2483C>T	NP_055423.1:p.Ala828Val
XM_011543873.1:c.2882C>T	XP_011542175.1:p.Ala961Val
XM_011543874.1:c.2882C>T	XP_011542176.1:p.Ala961Val
XM_011543875.1:c.2882C>T	XP_011542177.1:p.Ala961Val
XM_011543876.1:c.2477C>T	XP_011542178.1:p.Ala826Val
NM_001033028.2:c.1190C>T	NP_001028200.1:p.Ala397Val
NM_001287810.3:c.2483C>T	NP_001274739.1:p.Ala828Val
NM_001324119.2:c.2585C>T	NP_001311048.1:p.Ala862Val
NM_001324120.2:c.2483C>T	NP_001311049.1:p.Ala828Val
NM_001324122.2:c.803C>T	NP_001311051.1:p.Ala268Val
NM_001324123.2:c.2483C>T	NP_001311052.1:p.Ala828Val
NM_001324124.2:c.2393C>T	NP_001311053.1:p.Ala798Val
NM_001324125.2:c.2117C>T	NP_001311054.1:p.Ala706Val
NM_001324126.2:c.2381C>T	NP_001311055.1:p.Ala794Val
NM_014608.5:c.2483C>T	NP_055423.1:p.Ala828Val
XM_011543873.3:c.2882C>T	XP_011542175.1:p.Ala961Val
XM_011543874.2:c.2882C>T	XP_011542176.1:p.Ala961Val
XM_011543876.3:c.2579C>T	XP_011542178.2:p.Ala860Val
XM_017022023.2:c.2984C>T	XP_016877512.1:p.Ala995Val
XM_017022024.2:c.2882C>T	XP_016877513.1:p.Ala961Val
XM_024449876.1:c.2882C>T	XP_024305644.1:p.Ala961Val
XM_024449877.1:c.2483C>T	XP_024305645.1:p.Ala828Val
NM_014608.6:c.2483C>T MANE Select	NP_055423.1:p.Ala828Val
NM_001287810.4:c.2483C>T	NP_001274739.1:p.Ala828Val
NM_001324122.3:c.803C>T	NP_001311051.1:p.Ala268Val
NM_001324123.3:c.2483C>T	NP_001311052.1:p.Ala828Val
NM_001324124.3:c.2393C>T	NP_001311053.1:p.Ala798Val
NM_001324125.3:c.2117C>T	NP_001311054.1:p.Ala706Val
NM_001324126.3:c.2381C>T	NP_001311055.1:p.Ala794Val
NM_001033028.3:c.1190C>T	NP_001028200.1:p.Ala397Val