Canonical Allele Identifier: CA2114959294

Gene: FGF14 FGF14-IT1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312700_102312703delinsTAGG , CM000675.2:g.102312700_102312703delinsTAGG	GRCh38
NC_000013.10:g.102965050_102965053delinsTAGG , CM000675.1:g.102965050_102965053delinsTAGG	GRCh37
NC_000013.9:g.101763051_101763054delinsTAGG	NCBI36
NG_008317.1:g.94072_94075delinsCCTA
NG_008317.2:g.94072_94075delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+88768_208+88771delinsCCTA (FGF14)	ENSP00000365301.3:n.208+88768_208+88771delinsCCTA
ENST00000418923.3:c.91+88768_91+88771delinsCCTA (FGF14)	ENSP00000516414.1:n.91+88768_91+88771delinsCCTA
ENST00000706491.1:c.208+88768_208+88771delinsCCTA (FGF14)	ENSP00000516413.1:n.208+88768_208+88771delinsCCTA
ENST00000706492.1:c.*12+81055_*12+81058delinsCCTA (FGF14)	ENSP00000516415.1:n.*12+81055_*12+81058delinsCCTA
ENST00000706493.1:c.*107+53742_*107+53745delinsCCTA (FGF14)	ENSP00000516416.1:n.*107+53742_*107+53745delinsCCTA
ENST00000706494.1:c.-60+53742_-60+53745delinsCCTA (FGF14)	ENSP00000516417.1:n.-60+53742_-60+53745delinsCCTA
ENST00000376131.8:c.208+88768_208+88771delinsCCTA (FGF14)	ENSP00000365301.3:n.208+88768_208+88771delinsCCTA
NM_175929.2:c.208+88768_208+88771delinsCCTA (FGF14)	NP_787125.1:n.208+88768_208+88771delinsCCTA
NR_036486.1:n.410-18663_410-18660delinsCCTA (FGF14-IT1)
NM_001321935.1:c.-60+4933_-60+4936delinsCCTA (FGF14)	NP_001308864.1:n.-60+4933_-60+4936delinsCCTA
NM_001321936.1:c.-324+4933_-324+4936delinsCCTA (FGF14)	NP_001308865.1:n.-324+4933_-324+4936delinsCCTA
NM_001321937.1:c.208+88768_208+88771delinsCCTA (FGF14)	NP_001308866.1:n.208+88768_208+88771delinsCCTA
NM_001321938.1:c.-225+88768_-225+88771delinsCCTA (FGF14)	NP_001308867.1:n.-225+88768_-225+88771delinsCCTA
NM_001321939.1:c.208+88768_208+88771delinsCCTA (FGF14)	NP_001308868.1:n.208+88768_208+88771delinsCCTA
NM_001321940.1:c.-225+88768_-225+88771delinsCCTA (FGF14)	NP_001308869.1:n.-225+88768_-225+88771delinsCCTA
NM_001321941.1:c.-60-18663_-60-18660delinsCCTA (FGF14)	NP_001308870.1:n.-60-18663_-60-18660delinsCCTA
NM_001321942.1:c.-60+81055_-60+81058delinsCCTA (FGF14)	NP_001308871.1:n.-60+81055_-60+81058delinsCCTA
NM_001321943.1:c.-171+88768_-171+88771delinsCCTA (FGF14)	NP_001308872.1:n.-171+88768_-171+88771delinsCCTA
NM_001321944.1:c.-324+88768_-324+88771delinsCCTA (FGF14)	NP_001308873.1:n.-324+88768_-324+88771delinsCCTA
NM_001321945.1:c.91+88768_91+88771delinsCCTA (FGF14)	NP_001308874.1:n.91+88768_91+88771delinsCCTA
NM_001321946.1:c.-60+53742_-60+53745delinsCCTA (FGF14)	NP_001308875.1:n.-60+53742_-60+53745delinsCCTA
NM_001321947.1:c.52+88768_52+88771delinsCCTA (FGF14)	NP_001308876.1:n.52+88768_52+88771delinsCCTA
NM_001321948.1:c.91+88768_91+88771delinsCCTA (FGF14)	NP_001308877.1:n.91+88768_91+88771delinsCCTA
NM_001321949.1:c.-60+53742_-60+53745delinsCCTA (FGF14)	NP_001308878.1:n.-60+53742_-60+53745delinsCCTA
XR_001750081.2:n.6248-43_6248-40delinsTAGG
NM_001321938.2:c.-225+88768_-225+88771delinsCCTA (FGF14)	NP_001308867.1:n.-225+88768_-225+88771delinsCCTA
NM_001321945.2:c.91+88768_91+88771delinsCCTA (FGF14)	NP_001308874.1:n.91+88768_91+88771delinsCCTA
NM_001321946.2:c.-60+53742_-60+53745delinsCCTA (FGF14)	NP_001308875.1:n.-60+53742_-60+53745delinsCCTA
NM_001321947.2:c.52+88768_52+88771delinsCCTA (FGF14)	NP_001308876.1:n.52+88768_52+88771delinsCCTA
NM_001321948.2:c.91+88768_91+88771delinsCCTA (FGF14)	NP_001308877.1:n.91+88768_91+88771delinsCCTA
NM_001321937.2:c.208+88768_208+88771delinsCCTA (FGF14)	NP_001308866.1:n.208+88768_208+88771delinsCCTA
NM_001321939.2:c.208+88768_208+88771delinsCCTA (FGF14)	NP_001308868.1:n.208+88768_208+88771delinsCCTA
NM_001321941.2:c.-60-18663_-60-18660delinsCCTA (FGF14)	NP_001308870.1:n.-60-18663_-60-18660delinsCCTA
NM_001379342.1:c.91+88768_91+88771delinsCCTA (FGF14)	NP_001366271.1:n.91+88768_91+88771delinsCCTA
NM_175929.3:c.208+88768_208+88771delinsCCTA (FGF14)	NP_787125.1:n.208+88768_208+88771delinsCCTA