Canonical Allele Identifier: CA2800396836

Gene: FGF14 FGF14-IT1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312200_102312201del , CM000675.2:g.102312200_102312201del	GRCh38
NC_000013.10:g.102964550_102964551del , CM000675.1:g.102964550_102964551del	GRCh37
NC_000013.9:g.101762551_101762552del	NCBI36
NG_008317.1:g.94574_94575del
NG_008317.2:g.94574_94575del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+89270_208+89271del (FGF14)	ENSP00000365301.3:n.208+89270_208+89271del
ENST00000418923.3:c.91+89270_91+89271del (FGF14)	ENSP00000516414.1:n.91+89270_91+89271del
ENST00000706491.1:c.208+89270_208+89271del (FGF14)	ENSP00000516413.1:n.208+89270_208+89271del
ENST00000706492.1:c.*12+81557_*12+81558del (FGF14)	ENSP00000516415.1:n.*12+81557_*12+81558del
ENST00000706493.1:c.*107+54244_*107+54245del (FGF14)	ENSP00000516416.1:n.*107+54244_*107+54245del
ENST00000706494.1:c.-60+54244_-60+54245del (FGF14)	ENSP00000516417.1:n.-60+54244_-60+54245del
ENST00000376131.8:c.208+89270_208+89271del (FGF14)	ENSP00000365301.3:n.208+89270_208+89271del
NM_175929.2:c.208+89270_208+89271del (FGF14)	NP_787125.1:n.208+89270_208+89271del
NR_036486.1:n.410-18161_410-18160del (FGF14-IT1)
NM_001321935.1:c.-60+5435_-60+5436del (FGF14)	NP_001308864.1:n.-60+5435_-60+5436del
NM_001321936.1:c.-324+5435_-324+5436del (FGF14)	NP_001308865.1:n.-324+5435_-324+5436del
NM_001321937.1:c.208+89270_208+89271del (FGF14)	NP_001308866.1:n.208+89270_208+89271del
NM_001321938.1:c.-225+89270_-225+89271del (FGF14)	NP_001308867.1:n.-225+89270_-225+89271del
NM_001321939.1:c.208+89270_208+89271del (FGF14)	NP_001308868.1:n.208+89270_208+89271del
NM_001321940.1:c.-225+89270_-225+89271del (FGF14)	NP_001308869.1:n.-225+89270_-225+89271del
NM_001321941.1:c.-60-18161_-60-18160del (FGF14)	NP_001308870.1:n.-60-18161_-60-18160del
NM_001321942.1:c.-60+81557_-60+81558del (FGF14)	NP_001308871.1:n.-60+81557_-60+81558del
NM_001321943.1:c.-171+89270_-171+89271del (FGF14)	NP_001308872.1:n.-171+89270_-171+89271del
NM_001321944.1:c.-324+89270_-324+89271del (FGF14)	NP_001308873.1:n.-324+89270_-324+89271del
NM_001321945.1:c.91+89270_91+89271del (FGF14)	NP_001308874.1:n.91+89270_91+89271del
NM_001321946.1:c.-60+54244_-60+54245del (FGF14)	NP_001308875.1:n.-60+54244_-60+54245del
NM_001321947.1:c.52+89270_52+89271del (FGF14)	NP_001308876.1:n.52+89270_52+89271del
NM_001321948.1:c.91+89270_91+89271del (FGF14)	NP_001308877.1:n.91+89270_91+89271del
NM_001321949.1:c.-60+54244_-60+54245del (FGF14)	NP_001308878.1:n.-60+54244_-60+54245del
XR_001750081.2:n.6248-543_6248-542del
NM_001321938.2:c.-225+89270_-225+89271del (FGF14)	NP_001308867.1:n.-225+89270_-225+89271del
NM_001321945.2:c.91+89270_91+89271del (FGF14)	NP_001308874.1:n.91+89270_91+89271del
NM_001321946.2:c.-60+54244_-60+54245del (FGF14)	NP_001308875.1:n.-60+54244_-60+54245del
NM_001321947.2:c.52+89270_52+89271del (FGF14)	NP_001308876.1:n.52+89270_52+89271del
NM_001321948.2:c.91+89270_91+89271del (FGF14)	NP_001308877.1:n.91+89270_91+89271del
NM_001321937.2:c.208+89270_208+89271del (FGF14)	NP_001308866.1:n.208+89270_208+89271del
NM_001321939.2:c.208+89270_208+89271del (FGF14)	NP_001308868.1:n.208+89270_208+89271del
NM_001321941.2:c.-60-18161_-60-18160del (FGF14)	NP_001308870.1:n.-60-18161_-60-18160del
NM_001379342.1:c.91+89270_91+89271del (FGF14)	NP_001366271.1:n.91+89270_91+89271del
NM_175929.3:c.208+89270_208+89271del (FGF14)	NP_787125.1:n.208+89270_208+89271del