Canonical Allele Identifier: CA388711342
Gene: FGF14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101726769A>T , CM000675.2:g.101726769A>T GRCh38
NC_000013.10:g.102379119A>T , CM000675.1:g.102379119A>T GRCh37
NC_000013.9:g.101177120A>T NCBI36
NG_008317.1:g.680006T>A
NG_008317.2:g.680006T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376131.9:c.465T>A ENSP00000365301.3:p.Phe155Leu
ENST00000418923.3:c.348T>A ENSP00000516414.1:p.Phe116Leu
ENST00000706491.1:c.*54T>A ENSP00000516413.1:n.*54T>A
ENST00000706492.1:c.*269T>A ENSP00000516415.1:n.*269T>A
ENST00000706493.1:c.*364T>A ENSP00000516416.1:n.*364T>A
ENST00000706494.1:c.198T>A ENSP00000516417.1:p.Phe66Leu
ENST00000376143.5:c.450T>A MANE Select ENSP00000365313.4:p.Phe150Leu
ENST00000376131.8:c.465T>A ENSP00000365301.3:p.Phe155Leu
ENST00000376143.4:c.450T>A ENSP00000365313.4:p.Phe150Leu
NM_004115.3:c.450T>A NP_004106.1:p.Phe150Leu
NM_175929.2:c.465T>A NP_787125.1:p.Phe155Leu
XM_011521053.1:c.270T>A XP_011519355.1:p.Phe90Leu
NM_001321931.1:c.198T>A NP_001308860.1:p.Phe66Leu
NM_001321932.1:c.261T>A NP_001308861.1:p.Phe87Leu
NM_001321933.1:c.270T>A NP_001308862.1:p.Phe90Leu
NM_001321934.1:c.198T>A NP_001308863.1:p.Phe66Leu
NM_001321935.1:c.198T>A NP_001308864.1:p.Phe66Leu
NM_001321936.1:c.261T>A NP_001308865.1:p.Phe87Leu
NM_001321938.1:c.270T>A NP_001308867.1:p.Phe90Leu
NM_001321939.1:c.354T>A NP_001308868.1:p.Phe118Leu
NM_001321940.1:c.270T>A NP_001308869.1:p.Phe90Leu
NM_001321941.1:c.264T>A NP_001308870.1:p.Phe88Leu
NM_001321942.1:c.198T>A NP_001308871.1:p.Phe66Leu
NM_001321943.1:c.198T>A NP_001308872.1:p.Phe66Leu
NM_001321944.1:c.261T>A NP_001308873.1:p.Phe87Leu
NM_001321945.1:c.348T>A NP_001308874.1:p.Phe116Leu
NM_001321946.1:c.198T>A NP_001308875.1:p.Phe66Leu
NM_001321947.1:c.309T>A NP_001308876.1:p.Phe103Leu
NM_001321948.1:c.348T>A NP_001308877.1:p.Phe116Leu
NM_001321949.1:c.198T>A NP_001308878.1:p.Phe66Leu
NM_001321938.2:c.270T>A NP_001308867.1:p.Phe90Leu
NM_001321945.2:c.348T>A NP_001308874.1:p.Phe116Leu
NM_001321946.2:c.198T>A NP_001308875.1:p.Phe66Leu
NM_001321947.2:c.309T>A NP_001308876.1:p.Phe103Leu
NM_001321948.2:c.348T>A NP_001308877.1:p.Phe116Leu
NM_001321939.2:c.354T>A NP_001308868.1:p.Phe118Leu
NM_001321941.2:c.264T>A NP_001308870.1:p.Phe88Leu
NM_001379342.1:c.348T>A NP_001366271.1:p.Phe116Leu
NM_004115.4:c.450T>A MANE Select NP_004106.1:p.Phe150Leu
NM_175929.3:c.465T>A NP_787125.1:p.Phe155Leu