Canonical Allele Identifier: CA2114959282
Gene: FGF14 HGNC NCBI
FGF14-IT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102312684_102312687delinsTAAG , CM000675.2:g.102312684_102312687delinsTAAG GRCh38
NC_000013.10:g.102965034_102965037delinsTAAG , CM000675.1:g.102965034_102965037delinsTAAG GRCh37
NC_000013.9:g.101763035_101763038delinsTAAG NCBI36
NG_008317.1:g.94088_94091delinsCTTA
NG_008317.2:g.94088_94091delinsCTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000376131.9:c.208+88784_208+88787delinsCTTA (FGF14) ENSP00000365301.3:n.208+88784_208+88787de...
ENST00000418923.3:c.91+88784_91+88787delinsCTTA (FGF14) ENSP00000516414.1:n.91+88784_91+88787deli...
ENST00000706491.1:c.208+88784_208+88787delinsCTTA (FGF14) ENSP00000516413.1:n.208+88784_208+88787de...
ENST00000706492.1:c.*12+81071_*12+81074delinsCTTA (FGF14) ENSP00000516415.1:n.*12+81071_*12+81074de...
ENST00000706493.1:c.*107+53758_*107+53761delinsCTTA (FGF14) ENSP00000516416.1:n.*107+53758_*107+53761...
ENST00000706494.1:c.-60+53758_-60+53761delinsCTTA (FGF14) ENSP00000516417.1:n.-60+53758_-60+53761de...
ENST00000376131.8:c.208+88784_208+88787delinsCTTA (FGF14) ENSP00000365301.3:n.208+88784_208+88787de...
NM_175929.2:c.208+88784_208+88787delinsCTTA (FGF14) NP_787125.1:n.208+88784_208+88787delinsCT...
NR_036486.1:n.410-18647_410-18644delinsCTTA (FGF14-IT1)
NM_001321935.1:c.-60+4949_-60+4952delinsCTTA (FGF14) NP_001308864.1:n.-60+4949_-60+4952delinsC...
NM_001321936.1:c.-324+4949_-324+4952delinsCTTA (FGF14) NP_001308865.1:n.-324+4949_-324+4952delin...
NM_001321937.1:c.208+88784_208+88787delinsCTTA (FGF14) NP_001308866.1:n.208+88784_208+88787delin...
NM_001321938.1:c.-225+88784_-225+88787delinsCTTA (FGF14) NP_001308867.1:n.-225+88784_-225+88787del...
NM_001321939.1:c.208+88784_208+88787delinsCTTA (FGF14) NP_001308868.1:n.208+88784_208+88787delin...
NM_001321940.1:c.-225+88784_-225+88787delinsCTTA (FGF14) NP_001308869.1:n.-225+88784_-225+88787del...
NM_001321941.1:c.-60-18647_-60-18644delinsCTTA (FGF14) NP_001308870.1:n.-60-18647_-60-18644delin...
NM_001321942.1:c.-60+81071_-60+81074delinsCTTA (FGF14) NP_001308871.1:n.-60+81071_-60+81074delin...
NM_001321943.1:c.-171+88784_-171+88787delinsCTTA (FGF14) NP_001308872.1:n.-171+88784_-171+88787del...
NM_001321944.1:c.-324+88784_-324+88787delinsCTTA (FGF14) NP_001308873.1:n.-324+88784_-324+88787del...
NM_001321945.1:c.91+88784_91+88787delinsCTTA (FGF14) NP_001308874.1:n.91+88784_91+88787delinsC...
NM_001321946.1:c.-60+53758_-60+53761delinsCTTA (FGF14) NP_001308875.1:n.-60+53758_-60+53761delin...
NM_001321947.1:c.52+88784_52+88787delinsCTTA (FGF14) NP_001308876.1:n.52+88784_52+88787delinsC...
NM_001321948.1:c.91+88784_91+88787delinsCTTA (FGF14) NP_001308877.1:n.91+88784_91+88787delinsC...
NM_001321949.1:c.-60+53758_-60+53761delinsCTTA (FGF14) NP_001308878.1:n.-60+53758_-60+53761delin...
XR_001750081.2:n.6248-59_6248-56delinsTAAG
NM_001321938.2:c.-225+88784_-225+88787delinsCTTA (FGF14) NP_001308867.1:n.-225+88784_-225+88787del...
NM_001321945.2:c.91+88784_91+88787delinsCTTA (FGF14) NP_001308874.1:n.91+88784_91+88787delinsC...
NM_001321946.2:c.-60+53758_-60+53761delinsCTTA (FGF14) NP_001308875.1:n.-60+53758_-60+53761delin...
NM_001321947.2:c.52+88784_52+88787delinsCTTA (FGF14) NP_001308876.1:n.52+88784_52+88787delinsC...
NM_001321948.2:c.91+88784_91+88787delinsCTTA (FGF14) NP_001308877.1:n.91+88784_91+88787delinsC...
NM_001321937.2:c.208+88784_208+88787delinsCTTA (FGF14) NP_001308866.1:n.208+88784_208+88787delin...
NM_001321939.2:c.208+88784_208+88787delinsCTTA (FGF14) NP_001308868.1:n.208+88784_208+88787delin...
NM_001321941.2:c.-60-18647_-60-18644delinsCTTA (FGF14) NP_001308870.1:n.-60-18647_-60-18644delin...
NM_001379342.1:c.91+88784_91+88787delinsCTTA (FGF14) NP_001366271.1:n.91+88784_91+88787delinsC...
NM_175929.3:c.208+88784_208+88787delinsCTTA (FGF14) NP_787125.1:n.208+88784_208+88787delinsCT...