Canonical Allele Identifier: CA2114682845
Gene: FGF14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101726750A= , CM000675.2:g.101726750A= GRCh38
NC_000013.10:g.102379100A= , CM000675.1:g.102379100A= GRCh37
NC_000013.9:g.101177101A= NCBI36
NG_008317.1:g.680025T=
NG_008317.2:g.680025T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376131.9:c.484T= ENSP00000365301.3:p.Tyr162=
ENST00000418923.3:c.367T= ENSP00000516414.1:p.Tyr123=
ENST00000706491.1:c.*73T= ENSP00000516413.1:n.*73T=
ENST00000706492.1:c.*288T= ENSP00000516415.1:n.*288T=
ENST00000706493.1:c.*383T= ENSP00000516416.1:n.*383T=
ENST00000706494.1:c.217T= ENSP00000516417.1:p.Tyr73=
ENST00000376143.5:c.469T= MANE Select ENSP00000365313.4:p.Tyr157=
ENST00000376131.8:c.484T= ENSP00000365301.3:p.Tyr162=
ENST00000376143.4:c.469T= ENSP00000365313.4:p.Tyr157=
NM_004115.3:c.469T= NP_004106.1:p.Tyr157=
NM_175929.2:c.484T= NP_787125.1:p.Tyr162=
XM_011521053.1:c.289T= XP_011519355.1:p.Tyr97=
NM_001321931.1:c.217T= NP_001308860.1:p.Tyr73=
NM_001321932.1:c.280T= NP_001308861.1:p.Tyr94=
NM_001321933.1:c.289T= NP_001308862.1:p.Tyr97=
NM_001321934.1:c.217T= NP_001308863.1:p.Tyr73=
NM_001321935.1:c.217T= NP_001308864.1:p.Tyr73=
NM_001321936.1:c.280T= NP_001308865.1:p.Tyr94=
NM_001321938.1:c.289T= NP_001308867.1:p.Tyr97=
NM_001321939.1:c.373T= NP_001308868.1:p.Tyr125=
NM_001321940.1:c.289T= NP_001308869.1:p.Tyr97=
NM_001321941.1:c.283T= NP_001308870.1:p.Tyr95=
NM_001321942.1:c.217T= NP_001308871.1:p.Tyr73=
NM_001321943.1:c.217T= NP_001308872.1:p.Tyr73=
NM_001321944.1:c.280T= NP_001308873.1:p.Tyr94=
NM_001321945.1:c.367T= NP_001308874.1:p.Tyr123=
NM_001321946.1:c.217T= NP_001308875.1:p.Tyr73=
NM_001321947.1:c.328T= NP_001308876.1:p.Tyr110=
NM_001321948.1:c.367T= NP_001308877.1:p.Tyr123=
NM_001321949.1:c.217T= NP_001308878.1:p.Tyr73=
NM_001321938.2:c.289T= NP_001308867.1:p.Tyr97=
NM_001321945.2:c.367T= NP_001308874.1:p.Tyr123=
NM_001321946.2:c.217T= NP_001308875.1:p.Tyr73=
NM_001321947.2:c.328T= NP_001308876.1:p.Tyr110=
NM_001321948.2:c.367T= NP_001308877.1:p.Tyr123=
NM_001321939.2:c.373T= NP_001308868.1:p.Tyr125=
NM_001321941.2:c.283T= NP_001308870.1:p.Tyr95=
NM_001379342.1:c.367T= NP_001366271.1:p.Tyr123=
NM_004115.4:c.469T= MANE Select NP_004106.1:p.Tyr157=
NM_175929.3:c.484T= NP_787125.1:p.Tyr162=