Canonical Allele Identifier: CA2114682811

Gene: FGF14

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726731_101726732delinsCT , CM000675.2:g.101726731_101726732delinsCT	GRCh38
NC_000013.10:g.102379081_102379082delinsCT , CM000675.1:g.102379081_102379082delinsCT	GRCh37
NC_000013.9:g.101177082_101177083delinsCT	NCBI36
NG_008317.1:g.680043_680044delinsAG
NG_008317.2:g.680043_680044delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.502_503delinsAG	ENSP00000365301.3:p.Arg168=
ENST00000418923.3:c.385_386delinsAG	ENSP00000516414.1:p.Arg129=
ENST00000706491.1:c.*91_*92delinsAG	ENSP00000516413.1:n.*91_*92delinsAG
ENST00000706492.1:c.*306_*307delinsAG	ENSP00000516415.1:n.*306_*307delinsAG
ENST00000706493.1:c.*401_*402delinsAG	ENSP00000516416.1:n.*401_*402delinsAG
ENST00000706494.1:c.235_236delinsAG	ENSP00000516417.1:p.Arg79=
ENST00000376143.5:c.487_488delinsAG MANE Select	ENSP00000365313.4:p.Arg163=
ENST00000376131.8:c.502_503delinsAG	ENSP00000365301.3:p.Arg168=
ENST00000376143.4:c.487_488delinsAG	ENSP00000365313.4:p.Arg163=
NM_004115.3:c.487_488delinsAG	NP_004106.1:p.Arg163=
NM_175929.2:c.502_503delinsAG	NP_787125.1:p.Arg168=
XM_011521053.1:c.307_308delinsAG	XP_011519355.1:p.Arg103=
NM_001321931.1:c.235_236delinsAG	NP_001308860.1:p.Arg79=
NM_001321932.1:c.298_299delinsAG	NP_001308861.1:p.Arg100=
NM_001321933.1:c.307_308delinsAG	NP_001308862.1:p.Arg103=
NM_001321934.1:c.235_236delinsAG	NP_001308863.1:p.Arg79=
NM_001321935.1:c.235_236delinsAG	NP_001308864.1:p.Arg79=
NM_001321936.1:c.298_299delinsAG	NP_001308865.1:p.Arg100=
NM_001321938.1:c.307_308delinsAG	NP_001308867.1:p.Arg103=
NM_001321939.1:c.391_392delinsAG	NP_001308868.1:p.Arg131=
NM_001321940.1:c.307_308delinsAG	NP_001308869.1:p.Arg103=
NM_001321941.1:c.301_302delinsAG	NP_001308870.1:p.Arg101=
NM_001321942.1:c.235_236delinsAG	NP_001308871.1:p.Arg79=
NM_001321943.1:c.235_236delinsAG	NP_001308872.1:p.Arg79=
NM_001321944.1:c.298_299delinsAG	NP_001308873.1:p.Arg100=
NM_001321945.1:c.385_386delinsAG	NP_001308874.1:p.Arg129=
NM_001321946.1:c.235_236delinsAG	NP_001308875.1:p.Arg79=
NM_001321947.1:c.346_347delinsAG	NP_001308876.1:p.Arg116=
NM_001321948.1:c.385_386delinsAG	NP_001308877.1:p.Arg129=
NM_001321949.1:c.235_236delinsAG	NP_001308878.1:p.Arg79=
NM_001321938.2:c.307_308delinsAG	NP_001308867.1:p.Arg103=
NM_001321945.2:c.385_386delinsAG	NP_001308874.1:p.Arg129=
NM_001321946.2:c.235_236delinsAG	NP_001308875.1:p.Arg79=
NM_001321947.2:c.346_347delinsAG	NP_001308876.1:p.Arg116=
NM_001321948.2:c.385_386delinsAG	NP_001308877.1:p.Arg129=
NM_001321939.2:c.391_392delinsAG	NP_001308868.1:p.Arg131=
NM_001321941.2:c.301_302delinsAG	NP_001308870.1:p.Arg101=
NM_001379342.1:c.385_386delinsAG	NP_001366271.1:p.Arg129=
NM_004115.4:c.487_488delinsAG MANE Select	NP_004106.1:p.Arg163=
NM_175929.3:c.502_503delinsAG	NP_787125.1:p.Arg168=