Canonical Allele Identifier: CA2114682891

Gene: FGF14

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726785A= , CM000675.2:g.101726785A=	GRCh38
NC_000013.10:g.102379135A= , CM000675.1:g.102379135A=	GRCh37
NC_000013.9:g.101177136A=	NCBI36
NG_008317.1:g.679990T=
NG_008317.2:g.679990T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.449T=	ENSP00000365301.3:p.Phe150=
ENST00000418923.3:c.332T=	ENSP00000516414.1:p.Phe111=
ENST00000706491.1:c.*38T=	ENSP00000516413.1:n.*38T=
ENST00000706492.1:c.*253T=	ENSP00000516415.1:n.*253T=
ENST00000706493.1:c.*348T=	ENSP00000516416.1:n.*348T=
ENST00000706494.1:c.182T=	ENSP00000516417.1:p.Phe61=
ENST00000376143.5:c.434T= MANE Select	ENSP00000365313.4:p.Phe145=
ENST00000376131.8:c.449T=	ENSP00000365301.3:p.Phe150=
ENST00000376143.4:c.434T=	ENSP00000365313.4:p.Phe145=
NM_004115.3:c.434T=	NP_004106.1:p.Phe145=
NM_175929.2:c.449T=	NP_787125.1:p.Phe150=
XM_011521053.1:c.254T=	XP_011519355.1:p.Phe85=
NM_001321931.1:c.182T=	NP_001308860.1:p.Phe61=
NM_001321932.1:c.245T=	NP_001308861.1:p.Phe82=
NM_001321933.1:c.254T=	NP_001308862.1:p.Phe85=
NM_001321934.1:c.182T=	NP_001308863.1:p.Phe61=
NM_001321935.1:c.182T=	NP_001308864.1:p.Phe61=
NM_001321936.1:c.245T=	NP_001308865.1:p.Phe82=
NM_001321938.1:c.254T=	NP_001308867.1:p.Phe85=
NM_001321939.1:c.338T=	NP_001308868.1:p.Phe113=
NM_001321940.1:c.254T=	NP_001308869.1:p.Phe85=
NM_001321941.1:c.248T=	NP_001308870.1:p.Phe83=
NM_001321942.1:c.182T=	NP_001308871.1:p.Phe61=
NM_001321943.1:c.182T=	NP_001308872.1:p.Phe61=
NM_001321944.1:c.245T=	NP_001308873.1:p.Phe82=
NM_001321945.1:c.332T=	NP_001308874.1:p.Phe111=
NM_001321946.1:c.182T=	NP_001308875.1:p.Phe61=
NM_001321947.1:c.293T=	NP_001308876.1:p.Phe98=
NM_001321948.1:c.332T=	NP_001308877.1:p.Phe111=
NM_001321949.1:c.182T=	NP_001308878.1:p.Phe61=
NM_001321938.2:c.254T=	NP_001308867.1:p.Phe85=
NM_001321945.2:c.332T=	NP_001308874.1:p.Phe111=
NM_001321946.2:c.182T=	NP_001308875.1:p.Phe61=
NM_001321947.2:c.293T=	NP_001308876.1:p.Phe98=
NM_001321948.2:c.332T=	NP_001308877.1:p.Phe111=
NM_001321939.2:c.338T=	NP_001308868.1:p.Phe113=
NM_001321941.2:c.248T=	NP_001308870.1:p.Phe83=
NM_001379342.1:c.332T=	NP_001366271.1:p.Phe111=
NM_004115.4:c.434T= MANE Select	NP_004106.1:p.Phe145=
NM_175929.3:c.449T=	NP_787125.1:p.Phe150=