Canonical Allele Identifier: CA2741349129
Gene: FGF14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101726771_101726772insTTGATAGGTCT , CM000675.2:g.101726771_101726772insTTGATAGGTCT GRCh38
NC_000013.10:g.102379121_102379122insTTGATAGGTCT , CM000675.1:g.102379121_102379122insTTGATAGGTCT GRCh37
NC_000013.9:g.101177122_101177123insTTGATAGGTCT NCBI36
NG_008317.1:g.680003_680004insAGACCTATCAA
NG_008317.2:g.680003_680004insAGACCTATCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376131.9:c.462_463insAGACCTATCAA ENSP00000365301.3:p.Phe155ArgfsTer10
ENST00000418923.3:c.345_346insAGACCTATCAA ENSP00000516414.1:p.Phe116ArgfsTer10
ENST00000706491.1:c.*51_*52insAGACCTATCAA ENSP00000516413.1:n.*51_*52insAGACCTATCAA
ENST00000706492.1:c.*266_*267insAGACCTATCAA ENSP00000516415.1:n.*266_*267insAGACCTATCAA
ENST00000706493.1:c.*361_*362insAGACCTATCAA ENSP00000516416.1:n.*361_*362insAGACCTATCAA
ENST00000706494.1:c.195_196insAGACCTATCAA ENSP00000516417.1:p.Phe66ArgfsTer10
ENST00000376143.5:c.447_448insAGACCTATCAA MANE Select ENSP00000365313.4:p.Phe150ArgfsTer10
ENST00000376131.8:c.462_463insAGACCTATCAA ENSP00000365301.3:p.Phe155ArgfsTer10
ENST00000376143.4:c.447_448insAGACCTATCAA ENSP00000365313.4:p.Phe150ArgfsTer10
NM_004115.3:c.447_448insAGACCTATCAA NP_004106.1:p.Phe150ArgfsTer10
NM_175929.2:c.462_463insAGACCTATCAA NP_787125.1:p.Phe155ArgfsTer10
XM_011521053.1:c.267_268insAGACCTATCAA XP_011519355.1:p.Phe90ArgfsTer10
NM_001321931.1:c.195_196insAGACCTATCAA NP_001308860.1:p.Phe66ArgfsTer10
NM_001321932.1:c.258_259insAGACCTATCAA NP_001308861.1:p.Phe87ArgfsTer10
NM_001321933.1:c.267_268insAGACCTATCAA NP_001308862.1:p.Phe90ArgfsTer10
NM_001321934.1:c.195_196insAGACCTATCAA NP_001308863.1:p.Phe66ArgfsTer10
NM_001321935.1:c.195_196insAGACCTATCAA NP_001308864.1:p.Phe66ArgfsTer10
NM_001321936.1:c.258_259insAGACCTATCAA NP_001308865.1:p.Phe87ArgfsTer10
NM_001321938.1:c.267_268insAGACCTATCAA NP_001308867.1:p.Phe90ArgfsTer10
NM_001321939.1:c.351_352insAGACCTATCAA NP_001308868.1:p.Phe118ArgfsTer10
NM_001321940.1:c.267_268insAGACCTATCAA NP_001308869.1:p.Phe90ArgfsTer10
NM_001321941.1:c.261_262insAGACCTATCAA NP_001308870.1:p.Phe88ArgfsTer10
NM_001321942.1:c.195_196insAGACCTATCAA NP_001308871.1:p.Phe66ArgfsTer10
NM_001321943.1:c.195_196insAGACCTATCAA NP_001308872.1:p.Phe66ArgfsTer10
NM_001321944.1:c.258_259insAGACCTATCAA NP_001308873.1:p.Phe87ArgfsTer10
NM_001321945.1:c.345_346insAGACCTATCAA NP_001308874.1:p.Phe116ArgfsTer10
NM_001321946.1:c.195_196insAGACCTATCAA NP_001308875.1:p.Phe66ArgfsTer10
NM_001321947.1:c.306_307insAGACCTATCAA NP_001308876.1:p.Phe103ArgfsTer10
NM_001321948.1:c.345_346insAGACCTATCAA NP_001308877.1:p.Phe116ArgfsTer10
NM_001321949.1:c.195_196insAGACCTATCAA NP_001308878.1:p.Phe66ArgfsTer10
NM_001321938.2:c.267_268insAGACCTATCAA NP_001308867.1:p.Phe90ArgfsTer10
NM_001321945.2:c.345_346insAGACCTATCAA NP_001308874.1:p.Phe116ArgfsTer10
NM_001321946.2:c.195_196insAGACCTATCAA NP_001308875.1:p.Phe66ArgfsTer10
NM_001321947.2:c.306_307insAGACCTATCAA NP_001308876.1:p.Phe103ArgfsTer10
NM_001321948.2:c.345_346insAGACCTATCAA NP_001308877.1:p.Phe116ArgfsTer10
NM_001321939.2:c.351_352insAGACCTATCAA NP_001308868.1:p.Phe118ArgfsTer10
NM_001321941.2:c.261_262insAGACCTATCAA NP_001308870.1:p.Phe88ArgfsTer10
NM_001379342.1:c.345_346insAGACCTATCAA NP_001366271.1:p.Phe116ArgfsTer10
NM_004115.4:c.447_448insAGACCTATCAA MANE Select NP_004106.1:p.Phe150ArgfsTer10
NM_175929.3:c.462_463insAGACCTATCAA NP_787125.1:p.Phe155ArgfsTer10