Canonical Allele Identifier: CA959615158
Gene: FGF14 HGNC NCBI
FGF14-IT1 HGNC NCBI

Linked Data

dbSNP Id: rs1020984446

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102312747T>G , CM000675.2:g.102312747T>G GRCh38
NC_000013.10:g.102965097T>G , CM000675.1:g.102965097T>G GRCh37
NC_000013.9:g.101763098T>G NCBI36
NG_008317.1:g.94028A>C
NG_008317.2:g.94028A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376131.9:c.208+88724A>C (FGF14) ENSP00000365301.3:n.208+88724A>C
ENST00000418923.3:c.91+88724A>C (FGF14) ENSP00000516414.1:n.91+88724A>C
ENST00000706491.1:c.208+88724A>C (FGF14) ENSP00000516413.1:n.208+88724A>C
ENST00000706492.1:c.*12+81011A>C (FGF14) ENSP00000516415.1:n.*12+81011A>C
ENST00000706493.1:c.*107+53698A>C (FGF14) ENSP00000516416.1:n.*107+53698A>C
ENST00000706494.1:c.-60+53698A>C (FGF14) ENSP00000516417.1:n.-60+53698A>C
ENST00000376131.8:c.208+88724A>C (FGF14) ENSP00000365301.3:n.208+88724A>C
NM_175929.2:c.208+88724A>C (FGF14) NP_787125.1:n.208+88724A>C
NR_036486.1:n.410-18707A>C (FGF14-IT1)
NM_001321935.1:c.-60+4889A>C (FGF14) NP_001308864.1:n.-60+4889A>C
NM_001321936.1:c.-324+4889A>C (FGF14) NP_001308865.1:n.-324+4889A>C
NM_001321937.1:c.208+88724A>C (FGF14) NP_001308866.1:n.208+88724A>C
NM_001321938.1:c.-225+88724A>C (FGF14) NP_001308867.1:n.-225+88724A>C
NM_001321939.1:c.208+88724A>C (FGF14) NP_001308868.1:n.208+88724A>C
NM_001321940.1:c.-225+88724A>C (FGF14) NP_001308869.1:n.-225+88724A>C
NM_001321941.1:c.-60-18707A>C (FGF14) NP_001308870.1:n.-60-18707A>C
NM_001321942.1:c.-60+81011A>C (FGF14) NP_001308871.1:n.-60+81011A>C
NM_001321943.1:c.-171+88724A>C (FGF14) NP_001308872.1:n.-171+88724A>C
NM_001321944.1:c.-324+88724A>C (FGF14) NP_001308873.1:n.-324+88724A>C
NM_001321945.1:c.91+88724A>C (FGF14) NP_001308874.1:n.91+88724A>C
NM_001321946.1:c.-60+53698A>C (FGF14) NP_001308875.1:n.-60+53698A>C
NM_001321947.1:c.52+88724A>C (FGF14) NP_001308876.1:n.52+88724A>C
NM_001321948.1:c.91+88724A>C (FGF14) NP_001308877.1:n.91+88724A>C
NM_001321949.1:c.-60+53698A>C (FGF14) NP_001308878.1:n.-60+53698A>C
XR_001750081.2:n.6252T>G
NM_001321938.2:c.-225+88724A>C (FGF14) NP_001308867.1:n.-225+88724A>C
NM_001321945.2:c.91+88724A>C (FGF14) NP_001308874.1:n.91+88724A>C
NM_001321946.2:c.-60+53698A>C (FGF14) NP_001308875.1:n.-60+53698A>C
NM_001321947.2:c.52+88724A>C (FGF14) NP_001308876.1:n.52+88724A>C
NM_001321948.2:c.91+88724A>C (FGF14) NP_001308877.1:n.91+88724A>C
NM_001321937.2:c.208+88724A>C (FGF14) NP_001308866.1:n.208+88724A>C
NM_001321939.2:c.208+88724A>C (FGF14) NP_001308868.1:n.208+88724A>C
NM_001321941.2:c.-60-18707A>C (FGF14) NP_001308870.1:n.-60-18707A>C
NM_001379342.1:c.91+88724A>C (FGF14) NP_001366271.1:n.91+88724A>C
NM_175929.3:c.208+88724A>C (FGF14) NP_787125.1:n.208+88724A>C