Canonical Allele Identifier: CA711269642

Gene: CYFIP1

Linked Data

• dbSNP Id: rs1373257754
• gnomAD v3: 15-22903621-G-GGACCT
• gnomAD v4: 15-22903621-G-GGACCT
• MyVariant Identifiers: chr15:g.22903621_22903622insGACCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22903623_22903627dup , CM000677.2:g.22903623_22903627dup	GRCh38
NC_000015.9:g.22969442_22969446dup , CM000677.1:g.22969442_22969446dup	GRCh37
NC_000015.8:g.20520883_20520887dup	NCBI36
NG_054889.1:g.82281_82285dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612288.2:c.2582+80_2582+84dup	ENSP00000479802.2:n.2582+80_2582+84dup
ENST00000617928.5:c.2588+80_2588+84dup MANE Select	ENSP00000481038.1:n.2588+80_2588+84dup
ENST00000610365.4:c.2588+80_2588+84dup	ENSP00000478779.1:n.2588+80_2588+84dup
ENST00000617556.4:c.1295+80_1295+84dup	ENSP00000480525.1:n.1295+80_1295+84dup
ENST00000617928.4:c.2588+80_2588+84dup	ENSP00000481038.1:n.2588+80_2588+84dup
ENST00000619348.4:n.1735+80_1735+84dup
NM_001033028.1:c.1295+80_1295+84dup	NP_001028200.1:n.1295+80_1295+84dup
NM_001287810.1:c.2588+80_2588+84dup	NP_001274739.1:n.2588+80_2588+84dup
NM_014608.3:c.2588+80_2588+84dup	NP_055423.1:n.2588+80_2588+84dup
XM_011543873.1:c.2987+80_2987+84dup	XP_011542175.1:n.2987+80_2987+84dup
XM_011543874.1:c.2987+80_2987+84dup	XP_011542176.1:n.2987+80_2987+84dup
XM_011543875.1:c.2987+80_2987+84dup	XP_011542177.1:n.2987+80_2987+84dup
XM_011543876.1:c.2582+80_2582+84dup	XP_011542178.1:n.2582+80_2582+84dup
NM_001033028.2:c.1295+80_1295+84dup	NP_001028200.1:n.1295+80_1295+84dup
NM_001287810.3:c.2588+80_2588+84dup	NP_001274739.1:n.2588+80_2588+84dup
NM_001324119.2:c.2690+80_2690+84dup	NP_001311048.1:n.2690+80_2690+84dup
NM_001324120.2:c.2588+80_2588+84dup	NP_001311049.1:n.2588+80_2588+84dup
NM_001324122.2:c.908+80_908+84dup	NP_001311051.1:n.908+80_908+84dup
NM_001324123.2:c.2588+80_2588+84dup	NP_001311052.1:n.2588+80_2588+84dup
NM_001324124.2:c.2498+80_2498+84dup	NP_001311053.1:n.2498+80_2498+84dup
NM_001324125.2:c.2222+80_2222+84dup	NP_001311054.1:n.2222+80_2222+84dup
NM_001324126.2:c.2486+80_2486+84dup	NP_001311055.1:n.2486+80_2486+84dup
NM_014608.5:c.2588+80_2588+84dup	NP_055423.1:n.2588+80_2588+84dup
XM_011543873.3:c.2987+80_2987+84dup	XP_011542175.1:n.2987+80_2987+84dup
XM_011543874.2:c.2987+80_2987+84dup	XP_011542176.1:n.2987+80_2987+84dup
XM_011543876.3:c.2684+80_2684+84dup	XP_011542178.2:n.2684+80_2684+84dup
XM_017022023.2:c.3089+80_3089+84dup	XP_016877512.1:n.3089+80_3089+84dup
XM_017022024.2:c.2987+80_2987+84dup	XP_016877513.1:n.2987+80_2987+84dup
XM_024449876.1:c.2987+80_2987+84dup	XP_024305644.1:n.2987+80_2987+84dup
XM_024449877.1:c.2588+80_2588+84dup	XP_024305645.1:n.2588+80_2588+84dup
NM_014608.6:c.2588+80_2588+84dup MANE Select	NP_055423.1:n.2588+80_2588+84dup
NM_001287810.4:c.2588+80_2588+84dup	NP_001274739.1:n.2588+80_2588+84dup
NM_001324122.3:c.908+80_908+84dup	NP_001311051.1:n.908+80_908+84dup
NM_001324123.3:c.2588+80_2588+84dup	NP_001311052.1:n.2588+80_2588+84dup
NM_001324124.3:c.2498+80_2498+84dup	NP_001311053.1:n.2498+80_2498+84dup
NM_001324125.3:c.2222+80_2222+84dup	NP_001311054.1:n.2222+80_2222+84dup
NM_001324126.3:c.2486+80_2486+84dup	NP_001311055.1:n.2486+80_2486+84dup
NM_001033028.3:c.1295+80_1295+84dup	NP_001028200.1:n.1295+80_1295+84dup