Canonical Allele Identifier: CA2729145054

Gene: FGF14

Linked Data

• dbSNP Id: rs2139688463

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726702_101726703insGCC , CM000675.2:g.101726702_101726703insGCC	GRCh38
NC_000013.10:g.102379052_102379053insGCC , CM000675.1:g.102379052_102379053insGCC	GRCh37
NC_000013.9:g.101177053_101177054insGCC	NCBI36
NG_008317.1:g.680072_680073insGGC
NG_008317.2:g.680072_680073insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.531_532insGGC	ENSP00000365301.3:p.Phe177_Leu178insGly
ENST00000418923.3:c.414_415insGGC	ENSP00000516414.1:p.Phe138_Leu139insGly
ENST00000706491.1:c.*120_*121insGGC	ENSP00000516413.1:n.*120_*121insGGC
ENST00000706492.1:c.*335_*336insGGC	ENSP00000516415.1:n.*335_*336insGGC
ENST00000706493.1:c.*430_*431insGGC	ENSP00000516416.1:n.*430_*431insGGC
ENST00000706494.1:c.264_265insGGC	ENSP00000516417.1:p.Phe88_Leu89insGly
ENST00000376143.5:c.516_517insGGC MANE Select	ENSP00000365313.4:p.Phe172_Leu173insGly
ENST00000376131.8:c.531_532insGGC	ENSP00000365301.3:p.Phe177_Leu178insGly
ENST00000376143.4:c.516_517insGGC	ENSP00000365313.4:p.Phe172_Leu173insGly
NM_004115.3:c.516_517insGGC	NP_004106.1:p.Phe172_Leu173insGly
NM_175929.2:c.531_532insGGC	NP_787125.1:p.Phe177_Leu178insGly
XM_011521053.1:c.336_337insGGC	XP_011519355.1:p.Phe112_Leu113insGly
NM_001321931.1:c.264_265insGGC	NP_001308860.1:p.Phe88_Leu89insGly
NM_001321932.1:c.327_328insGGC	NP_001308861.1:p.Phe109_Leu110insGly
NM_001321933.1:c.336_337insGGC	NP_001308862.1:p.Phe112_Leu113insGly
NM_001321934.1:c.264_265insGGC	NP_001308863.1:p.Phe88_Leu89insGly
NM_001321935.1:c.264_265insGGC	NP_001308864.1:p.Phe88_Leu89insGly
NM_001321936.1:c.327_328insGGC	NP_001308865.1:p.Phe109_Leu110insGly
NM_001321938.1:c.336_337insGGC	NP_001308867.1:p.Phe112_Leu113insGly
NM_001321939.1:c.420_421insGGC	NP_001308868.1:p.Phe140_Leu141insGly
NM_001321940.1:c.336_337insGGC	NP_001308869.1:p.Phe112_Leu113insGly
NM_001321941.1:c.330_331insGGC	NP_001308870.1:p.Phe110_Leu111insGly
NM_001321942.1:c.264_265insGGC	NP_001308871.1:p.Phe88_Leu89insGly
NM_001321943.1:c.264_265insGGC	NP_001308872.1:p.Phe88_Leu89insGly
NM_001321944.1:c.327_328insGGC	NP_001308873.1:p.Phe109_Leu110insGly
NM_001321945.1:c.414_415insGGC	NP_001308874.1:p.Phe138_Leu139insGly
NM_001321946.1:c.264_265insGGC	NP_001308875.1:p.Phe88_Leu89insGly
NM_001321947.1:c.375_376insGGC	NP_001308876.1:p.Phe125_Leu126insGly
NM_001321948.1:c.414_415insGGC	NP_001308877.1:p.Phe138_Leu139insGly
NM_001321949.1:c.264_265insGGC	NP_001308878.1:p.Phe88_Leu89insGly
NM_001321938.2:c.336_337insGGC	NP_001308867.1:p.Phe112_Leu113insGly
NM_001321945.2:c.414_415insGGC	NP_001308874.1:p.Phe138_Leu139insGly
NM_001321946.2:c.264_265insGGC	NP_001308875.1:p.Phe88_Leu89insGly
NM_001321947.2:c.375_376insGGC	NP_001308876.1:p.Phe125_Leu126insGly
NM_001321948.2:c.414_415insGGC	NP_001308877.1:p.Phe138_Leu139insGly
NM_001321939.2:c.420_421insGGC	NP_001308868.1:p.Phe140_Leu141insGly
NM_001321941.2:c.330_331insGGC	NP_001308870.1:p.Phe110_Leu111insGly
NM_001379342.1:c.414_415insGGC	NP_001366271.1:p.Phe138_Leu139insGly
NM_004115.4:c.516_517insGGC MANE Select	NP_004106.1:p.Phe172_Leu173insGly
NM_175929.3:c.531_532insGGC	NP_787125.1:p.Phe177_Leu178insGly