Canonical Allele Identifier: CA488526508
Gene: CYFIP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.22969198C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22903870G>A , CM000677.2:g.22903870G>A GRCh38
NC_000015.9:g.22969198C>T , CM000677.1:g.22969198C>T GRCh37
NC_000015.8:g.20520639C>T NCBI36
NG_054889.1:g.82037C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000612288.2:c.2418C>T ENSP00000479802.2:p.Thr806=
ENST00000617928.5:c.2424C>T MANE Select ENSP00000481038.1:p.Thr808=
ENST00000610365.4:c.2424C>T ENSP00000478779.1:p.Thr808=
ENST00000617556.4:c.1131C>T ENSP00000480525.1:p.Thr377=
ENST00000617928.4:c.2424C>T ENSP00000481038.1:p.Thr808=
ENST00000619290.4:n.817C>T
ENST00000619348.4:n.1571C>T
NM_001033028.1:c.1131C>T NP_001028200.1:p.Thr377=
NM_001287810.1:c.2424C>T NP_001274739.1:p.Thr808=
NM_014608.3:c.2424C>T NP_055423.1:p.Thr808=
XM_011543873.1:c.2823C>T XP_011542175.1:p.Thr941=
XM_011543874.1:c.2823C>T XP_011542176.1:p.Thr941=
XM_011543875.1:c.2823C>T XP_011542177.1:p.Thr941=
XM_011543876.1:c.2418C>T XP_011542178.1:p.Thr806=
NM_001033028.2:c.1131C>T NP_001028200.1:p.Thr377=
NM_001287810.3:c.2424C>T NP_001274739.1:p.Thr808=
NM_001324119.2:c.2526C>T NP_001311048.1:p.Thr842=
NM_001324120.2:c.2424C>T NP_001311049.1:p.Thr808=
NM_001324122.2:c.744C>T NP_001311051.1:p.Thr248=
NM_001324123.2:c.2424C>T NP_001311052.1:p.Thr808=
NM_001324124.2:c.2334C>T NP_001311053.1:p.Thr778=
NM_001324125.2:c.2058C>T NP_001311054.1:p.Thr686=
NM_001324126.2:c.2322C>T NP_001311055.1:p.Thr774=
NM_014608.5:c.2424C>T NP_055423.1:p.Thr808=
XM_011543873.3:c.2823C>T XP_011542175.1:p.Thr941=
XM_011543874.2:c.2823C>T XP_011542176.1:p.Thr941=
XM_011543876.3:c.2520C>T XP_011542178.2:p.Thr840=
XM_017022023.2:c.2925C>T XP_016877512.1:p.Thr975=
XM_017022024.2:c.2823C>T XP_016877513.1:p.Thr941=
XM_024449876.1:c.2823C>T XP_024305644.1:p.Thr941=
XM_024449877.1:c.2424C>T XP_024305645.1:p.Thr808=
NM_014608.6:c.2424C>T MANE Select NP_055423.1:p.Thr808=
NM_001287810.4:c.2424C>T NP_001274739.1:p.Thr808=
NM_001324122.3:c.744C>T NP_001311051.1:p.Thr248=
NM_001324123.3:c.2424C>T NP_001311052.1:p.Thr808=
NM_001324124.3:c.2334C>T NP_001311053.1:p.Thr778=
NM_001324125.3:c.2058C>T NP_001311054.1:p.Thr686=
NM_001324126.3:c.2322C>T NP_001311055.1:p.Thr774=
NM_001033028.3:c.1131C>T NP_001028200.1:p.Thr377=