Canonical Allele Identifier: CA2114959258
Gene: FGF14 HGNC NCBI
FGF14-IT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102312634_102312635delinsCT , CM000675.2:g.102312634_102312635delinsCT GRCh38
NC_000013.10:g.102964984_102964985delinsCT , CM000675.1:g.102964984_102964985delinsCT GRCh37
NC_000013.9:g.101762985_101762986delinsCT NCBI36
NG_008317.1:g.94140_94141delinsAG
NG_008317.2:g.94140_94141delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376131.9:c.208+88836_208+88837delinsAG (FGF14) ENSP00000365301.3:n.208+88836_208+88837delinsAG
ENST00000418923.3:c.91+88836_91+88837delinsAG (FGF14) ENSP00000516414.1:n.91+88836_91+88837delinsAG
ENST00000706491.1:c.208+88836_208+88837delinsAG (FGF14) ENSP00000516413.1:n.208+88836_208+88837delinsAG
ENST00000706492.1:c.*12+81123_*12+81124delinsAG (FGF14) ENSP00000516415.1:n.*12+81123_*12+81124delinsAG
ENST00000706493.1:c.*107+53810_*107+53811delinsAG (FGF14) ENSP00000516416.1:n.*107+53810_*107+53811delinsAG
ENST00000706494.1:c.-60+53810_-60+53811delinsAG (FGF14) ENSP00000516417.1:n.-60+53810_-60+53811delinsAG
ENST00000376131.8:c.208+88836_208+88837delinsAG (FGF14) ENSP00000365301.3:n.208+88836_208+88837delinsAG
NM_175929.2:c.208+88836_208+88837delinsAG (FGF14) NP_787125.1:n.208+88836_208+88837delinsAG
NR_036486.1:n.410-18595_410-18594delinsAG (FGF14-IT1)
NM_001321935.1:c.-60+5001_-60+5002delinsAG (FGF14) NP_001308864.1:n.-60+5001_-60+5002delinsAG
NM_001321936.1:c.-324+5001_-324+5002delinsAG (FGF14) NP_001308865.1:n.-324+5001_-324+5002delinsAG
NM_001321937.1:c.208+88836_208+88837delinsAG (FGF14) NP_001308866.1:n.208+88836_208+88837delinsAG
NM_001321938.1:c.-225+88836_-225+88837delinsAG (FGF14) NP_001308867.1:n.-225+88836_-225+88837delinsAG
NM_001321939.1:c.208+88836_208+88837delinsAG (FGF14) NP_001308868.1:n.208+88836_208+88837delinsAG
NM_001321940.1:c.-225+88836_-225+88837delinsAG (FGF14) NP_001308869.1:n.-225+88836_-225+88837delinsAG
NM_001321941.1:c.-60-18595_-60-18594delinsAG (FGF14) NP_001308870.1:n.-60-18595_-60-18594delinsAG
NM_001321942.1:c.-60+81123_-60+81124delinsAG (FGF14) NP_001308871.1:n.-60+81123_-60+81124delinsAG
NM_001321943.1:c.-171+88836_-171+88837delinsAG (FGF14) NP_001308872.1:n.-171+88836_-171+88837delinsAG
NM_001321944.1:c.-324+88836_-324+88837delinsAG (FGF14) NP_001308873.1:n.-324+88836_-324+88837delinsAG
NM_001321945.1:c.91+88836_91+88837delinsAG (FGF14) NP_001308874.1:n.91+88836_91+88837delinsAG
NM_001321946.1:c.-60+53810_-60+53811delinsAG (FGF14) NP_001308875.1:n.-60+53810_-60+53811delinsAG
NM_001321947.1:c.52+88836_52+88837delinsAG (FGF14) NP_001308876.1:n.52+88836_52+88837delinsAG
NM_001321948.1:c.91+88836_91+88837delinsAG (FGF14) NP_001308877.1:n.91+88836_91+88837delinsAG
NM_001321949.1:c.-60+53810_-60+53811delinsAG (FGF14) NP_001308878.1:n.-60+53810_-60+53811delinsAG
XR_001750081.2:n.6248-109_6248-108delinsCT
NM_001321938.2:c.-225+88836_-225+88837delinsAG (FGF14) NP_001308867.1:n.-225+88836_-225+88837delinsAG
NM_001321945.2:c.91+88836_91+88837delinsAG (FGF14) NP_001308874.1:n.91+88836_91+88837delinsAG
NM_001321946.2:c.-60+53810_-60+53811delinsAG (FGF14) NP_001308875.1:n.-60+53810_-60+53811delinsAG
NM_001321947.2:c.52+88836_52+88837delinsAG (FGF14) NP_001308876.1:n.52+88836_52+88837delinsAG
NM_001321948.2:c.91+88836_91+88837delinsAG (FGF14) NP_001308877.1:n.91+88836_91+88837delinsAG
NM_001321937.2:c.208+88836_208+88837delinsAG (FGF14) NP_001308866.1:n.208+88836_208+88837delinsAG
NM_001321939.2:c.208+88836_208+88837delinsAG (FGF14) NP_001308868.1:n.208+88836_208+88837delinsAG
NM_001321941.2:c.-60-18595_-60-18594delinsAG (FGF14) NP_001308870.1:n.-60-18595_-60-18594delinsAG
NM_001379342.1:c.91+88836_91+88837delinsAG (FGF14) NP_001366271.1:n.91+88836_91+88837delinsAG
NM_175929.3:c.208+88836_208+88837delinsAG (FGF14) NP_787125.1:n.208+88836_208+88837delinsAG