Canonical Allele Identifier: CA2729145140

Gene: FGF14

Linked Data

• dbSNP Id: rs2139688913

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726760_101726761insGGAAGGGCAAGCTATGAAAGGGAACAGAG , CM000675.2:g.101726760_101726761insGGAAGGGCAAGCTATGAAAGGGAACAGAG	GRCh38
NC_000013.10:g.102379110_102379111insGGAAGGGCAAGCTATGAAAGGGAACAGAG , CM000675.1:g.102379110_102379111insGGAAGGGCAAGCTATGAAAGGGAACAGAG	GRCh37
NC_000013.9:g.101177111_101177112insGGAAGGGCAAGCTATGAAAGGGAACAGAG	NCBI36
NG_008317.1:g.680014_680015insCTCTGTTCCCTTTCATAGCTTGCCCTTCC
NG_008317.2:g.680014_680015insCTCTGTTCCCTTTCATAGCTTGCCCTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.473_474insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000365301.3:p.Tyr159SerfsTer12
ENST00000418923.3:c.356_357insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000516414.1:p.Tyr120SerfsTer12
ENST00000706491.1:c.*62_*63insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000516413.1:n.*62_*63insCTCTGTTCCCTTTCATAGCTTGCCCTTCC
ENST00000706492.1:c.*277_*278insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000516415.1:n.*277_*278insCTCTGTTCCCTTTCATAGCTTGCCCTTCC...
ENST00000706493.1:c.*372_*373insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000516416.1:n.*372_*373insCTCTGTTCCCTTTCATAGCTTGCCCTTCC...
ENST00000706494.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000516417.1:p.Tyr70SerfsTer12
ENST00000376143.5:c.458_459insCTCTGTTCCCTTTCATAGCTTGCCCTTCC MANE Select	ENSP00000365313.4:p.Tyr154SerfsTer12
ENST00000376131.8:c.473_474insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000365301.3:p.Tyr159SerfsTer12
ENST00000376143.4:c.458_459insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	ENSP00000365313.4:p.Tyr154SerfsTer12
NM_004115.3:c.458_459insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_004106.1:p.Tyr154SerfsTer12
NM_175929.2:c.473_474insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_787125.1:p.Tyr159SerfsTer12
XM_011521053.1:c.278_279insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	XP_011519355.1:p.Tyr94SerfsTer12
NM_001321931.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308860.1:p.Tyr70SerfsTer12
NM_001321932.1:c.269_270insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308861.1:p.Tyr91SerfsTer12
NM_001321933.1:c.278_279insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308862.1:p.Tyr94SerfsTer12
NM_001321934.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308863.1:p.Tyr70SerfsTer12
NM_001321935.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308864.1:p.Tyr70SerfsTer12
NM_001321936.1:c.269_270insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308865.1:p.Tyr91SerfsTer12
NM_001321938.1:c.278_279insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308867.1:p.Tyr94SerfsTer12
NM_001321939.1:c.362_363insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308868.1:p.Tyr122SerfsTer12
NM_001321940.1:c.278_279insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308869.1:p.Tyr94SerfsTer12
NM_001321941.1:c.272_273insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308870.1:p.Tyr92SerfsTer12
NM_001321942.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308871.1:p.Tyr70SerfsTer12
NM_001321943.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308872.1:p.Tyr70SerfsTer12
NM_001321944.1:c.269_270insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308873.1:p.Tyr91SerfsTer12
NM_001321945.1:c.356_357insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308874.1:p.Tyr120SerfsTer12
NM_001321946.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308875.1:p.Tyr70SerfsTer12
NM_001321947.1:c.317_318insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308876.1:p.Tyr107SerfsTer12
NM_001321948.1:c.356_357insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308877.1:p.Tyr120SerfsTer12
NM_001321949.1:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308878.1:p.Tyr70SerfsTer12
NM_001321938.2:c.278_279insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308867.1:p.Tyr94SerfsTer12
NM_001321945.2:c.356_357insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308874.1:p.Tyr120SerfsTer12
NM_001321946.2:c.206_207insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308875.1:p.Tyr70SerfsTer12
NM_001321947.2:c.317_318insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308876.1:p.Tyr107SerfsTer12
NM_001321948.2:c.356_357insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308877.1:p.Tyr120SerfsTer12
NM_001321939.2:c.362_363insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308868.1:p.Tyr122SerfsTer12
NM_001321941.2:c.272_273insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001308870.1:p.Tyr92SerfsTer12
NM_001379342.1:c.356_357insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_001366271.1:p.Tyr120SerfsTer12
NM_004115.4:c.458_459insCTCTGTTCCCTTTCATAGCTTGCCCTTCC MANE Select	NP_004106.1:p.Tyr154SerfsTer12
NM_175929.3:c.473_474insCTCTGTTCCCTTTCATAGCTTGCCCTTCC	NP_787125.1:p.Tyr159SerfsTer12