Canonical Allele Identifier: CA2114959098
Gene: FGF14 HGNC NCBI
FGF14-IT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102312220_102312221delinsAC , CM000675.2:g.102312220_102312221delinsAC GRCh38
NC_000013.10:g.102964570_102964571delinsAC , CM000675.1:g.102964570_102964571delinsAC GRCh37
NC_000013.9:g.101762571_101762572delinsAC NCBI36
NG_008317.1:g.94554_94555delinsGT
NG_008317.2:g.94554_94555delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376131.9:c.208+89250_208+89251delinsGT (FGF14) ENSP00000365301.3:n.208+89250_208+89251delinsGT
ENST00000418923.3:c.91+89250_91+89251delinsGT (FGF14) ENSP00000516414.1:n.91+89250_91+89251delinsGT
ENST00000706491.1:c.208+89250_208+89251delinsGT (FGF14) ENSP00000516413.1:n.208+89250_208+89251delinsGT
ENST00000706492.1:c.*12+81537_*12+81538delinsGT (FGF14) ENSP00000516415.1:n.*12+81537_*12+81538delinsGT
ENST00000706493.1:c.*107+54224_*107+54225delinsGT (FGF14) ENSP00000516416.1:n.*107+54224_*107+54225delinsGT
ENST00000706494.1:c.-60+54224_-60+54225delinsGT (FGF14) ENSP00000516417.1:n.-60+54224_-60+54225delinsGT
ENST00000376131.8:c.208+89250_208+89251delinsGT (FGF14) ENSP00000365301.3:n.208+89250_208+89251delinsGT
NM_175929.2:c.208+89250_208+89251delinsGT (FGF14) NP_787125.1:n.208+89250_208+89251delinsGT
NR_036486.1:n.410-18181_410-18180delinsGT (FGF14-IT1)
NM_001321935.1:c.-60+5415_-60+5416delinsGT (FGF14) NP_001308864.1:n.-60+5415_-60+5416delinsGT
NM_001321936.1:c.-324+5415_-324+5416delinsGT (FGF14) NP_001308865.1:n.-324+5415_-324+5416delinsGT
NM_001321937.1:c.208+89250_208+89251delinsGT (FGF14) NP_001308866.1:n.208+89250_208+89251delinsGT
NM_001321938.1:c.-225+89250_-225+89251delinsGT (FGF14) NP_001308867.1:n.-225+89250_-225+89251delinsGT
NM_001321939.1:c.208+89250_208+89251delinsGT (FGF14) NP_001308868.1:n.208+89250_208+89251delinsGT
NM_001321940.1:c.-225+89250_-225+89251delinsGT (FGF14) NP_001308869.1:n.-225+89250_-225+89251delinsGT
NM_001321941.1:c.-60-18181_-60-18180delinsGT (FGF14) NP_001308870.1:n.-60-18181_-60-18180delinsGT
NM_001321942.1:c.-60+81537_-60+81538delinsGT (FGF14) NP_001308871.1:n.-60+81537_-60+81538delinsGT
NM_001321943.1:c.-171+89250_-171+89251delinsGT (FGF14) NP_001308872.1:n.-171+89250_-171+89251delinsGT
NM_001321944.1:c.-324+89250_-324+89251delinsGT (FGF14) NP_001308873.1:n.-324+89250_-324+89251delinsGT
NM_001321945.1:c.91+89250_91+89251delinsGT (FGF14) NP_001308874.1:n.91+89250_91+89251delinsGT
NM_001321946.1:c.-60+54224_-60+54225delinsGT (FGF14) NP_001308875.1:n.-60+54224_-60+54225delinsGT
NM_001321947.1:c.52+89250_52+89251delinsGT (FGF14) NP_001308876.1:n.52+89250_52+89251delinsGT
NM_001321948.1:c.91+89250_91+89251delinsGT (FGF14) NP_001308877.1:n.91+89250_91+89251delinsGT
NM_001321949.1:c.-60+54224_-60+54225delinsGT (FGF14) NP_001308878.1:n.-60+54224_-60+54225delinsGT
XR_001750081.2:n.6248-523_6248-522delinsAC
NM_001321938.2:c.-225+89250_-225+89251delinsGT (FGF14) NP_001308867.1:n.-225+89250_-225+89251delinsGT
NM_001321945.2:c.91+89250_91+89251delinsGT (FGF14) NP_001308874.1:n.91+89250_91+89251delinsGT
NM_001321946.2:c.-60+54224_-60+54225delinsGT (FGF14) NP_001308875.1:n.-60+54224_-60+54225delinsGT
NM_001321947.2:c.52+89250_52+89251delinsGT (FGF14) NP_001308876.1:n.52+89250_52+89251delinsGT
NM_001321948.2:c.91+89250_91+89251delinsGT (FGF14) NP_001308877.1:n.91+89250_91+89251delinsGT
NM_001321937.2:c.208+89250_208+89251delinsGT (FGF14) NP_001308866.1:n.208+89250_208+89251delinsGT
NM_001321939.2:c.208+89250_208+89251delinsGT (FGF14) NP_001308868.1:n.208+89250_208+89251delinsGT
NM_001321941.2:c.-60-18181_-60-18180delinsGT (FGF14) NP_001308870.1:n.-60-18181_-60-18180delinsGT
NM_001379342.1:c.91+89250_91+89251delinsGT (FGF14) NP_001366271.1:n.91+89250_91+89251delinsGT
NM_175929.3:c.208+89250_208+89251delinsGT (FGF14) NP_787125.1:n.208+89250_208+89251delinsGT