Canonical Allele Identifier: CA2838308458

Gene: FGF14

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726759_101726760insG , CM000675.2:g.101726759_101726760insG	GRCh38
NC_000013.10:g.102379109_102379110insG , CM000675.1:g.102379109_102379110insG	GRCh37
NC_000013.9:g.101177110_101177111insG	NCBI36
NG_008317.1:g.680015_680016insC
NG_008317.2:g.680015_680016insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.474_475insC	ENSP00000365301.3:p.Tyr159LeufsTer16
ENST00000418923.3:c.357_358insC	ENSP00000516414.1:p.Tyr120LeufsTer16
ENST00000706491.1:c.*63_*64insC	ENSP00000516413.1:n.*63_*64insC
ENST00000706492.1:c.*278_*279insC	ENSP00000516415.1:n.*278_*279insC
ENST00000706493.1:c.*373_*374insC	ENSP00000516416.1:n.*373_*374insC
ENST00000706494.1:c.207_208insC	ENSP00000516417.1:p.Tyr70LeufsTer16
ENST00000376143.5:c.459_460insC MANE Select	ENSP00000365313.4:p.Tyr154LeufsTer16
ENST00000376131.8:c.474_475insC	ENSP00000365301.3:p.Tyr159LeufsTer16
ENST00000376143.4:c.459_460insC	ENSP00000365313.4:p.Tyr154LeufsTer16
NM_004115.3:c.459_460insC	NP_004106.1:p.Tyr154LeufsTer16
NM_175929.2:c.474_475insC	NP_787125.1:p.Tyr159LeufsTer16
XM_011521053.1:c.279_280insC	XP_011519355.1:p.Tyr94LeufsTer16
NM_001321931.1:c.207_208insC	NP_001308860.1:p.Tyr70LeufsTer16
NM_001321932.1:c.270_271insC	NP_001308861.1:p.Tyr91LeufsTer16
NM_001321933.1:c.279_280insC	NP_001308862.1:p.Tyr94LeufsTer16
NM_001321934.1:c.207_208insC	NP_001308863.1:p.Tyr70LeufsTer16
NM_001321935.1:c.207_208insC	NP_001308864.1:p.Tyr70LeufsTer16
NM_001321936.1:c.270_271insC	NP_001308865.1:p.Tyr91LeufsTer16
NM_001321938.1:c.279_280insC	NP_001308867.1:p.Tyr94LeufsTer16
NM_001321939.1:c.363_364insC	NP_001308868.1:p.Tyr122LeufsTer16
NM_001321940.1:c.279_280insC	NP_001308869.1:p.Tyr94LeufsTer16
NM_001321941.1:c.273_274insC	NP_001308870.1:p.Tyr92LeufsTer16
NM_001321942.1:c.207_208insC	NP_001308871.1:p.Tyr70LeufsTer16
NM_001321943.1:c.207_208insC	NP_001308872.1:p.Tyr70LeufsTer16
NM_001321944.1:c.270_271insC	NP_001308873.1:p.Tyr91LeufsTer16
NM_001321945.1:c.357_358insC	NP_001308874.1:p.Tyr120LeufsTer16
NM_001321946.1:c.207_208insC	NP_001308875.1:p.Tyr70LeufsTer16
NM_001321947.1:c.318_319insC	NP_001308876.1:p.Tyr107LeufsTer16
NM_001321948.1:c.357_358insC	NP_001308877.1:p.Tyr120LeufsTer16
NM_001321949.1:c.207_208insC	NP_001308878.1:p.Tyr70LeufsTer16
NM_001321938.2:c.279_280insC	NP_001308867.1:p.Tyr94LeufsTer16
NM_001321945.2:c.357_358insC	NP_001308874.1:p.Tyr120LeufsTer16
NM_001321946.2:c.207_208insC	NP_001308875.1:p.Tyr70LeufsTer16
NM_001321947.2:c.318_319insC	NP_001308876.1:p.Tyr107LeufsTer16
NM_001321948.2:c.357_358insC	NP_001308877.1:p.Tyr120LeufsTer16
NM_001321939.2:c.363_364insC	NP_001308868.1:p.Tyr122LeufsTer16
NM_001321941.2:c.273_274insC	NP_001308870.1:p.Tyr92LeufsTer16
NM_001379342.1:c.357_358insC	NP_001366271.1:p.Tyr120LeufsTer16
NM_004115.4:c.459_460insC MANE Select	NP_004106.1:p.Tyr154LeufsTer16
NM_175929.3:c.474_475insC	NP_787125.1:p.Tyr159LeufsTer16