Canonical Allele Identifier: CA2800396856

Gene: FGF14 FGF14-IT1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312784_102312785insCAAGAA , CM000675.2:g.102312784_102312785insCAAGAA	GRCh38
NC_000013.10:g.102965134_102965135insCAAGAA , CM000675.1:g.102965134_102965135insCAAGAA	GRCh37
NC_000013.9:g.101763135_101763136insCAAGAA	NCBI36
NG_008317.1:g.93990_93991insTTCTTG
NG_008317.2:g.93990_93991insTTCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+88686_208+88687insTTCTTG (FGF14)	ENSP00000365301.3:n.208+88686_208+88687insTTCTTG
ENST00000418923.3:c.91+88686_91+88687insTTCTTG (FGF14)	ENSP00000516414.1:n.91+88686_91+88687insTTCTTG
ENST00000706491.1:c.208+88686_208+88687insTTCTTG (FGF14)	ENSP00000516413.1:n.208+88686_208+88687insTTCTTG
ENST00000706492.1:c.*12+80973_*12+80974insTTCTTG (FGF14)	ENSP00000516415.1:n.*12+80973_*12+80974insTTCTTG
ENST00000706493.1:c.*107+53660_*107+53661insTTCTTG (FGF14)	ENSP00000516416.1:n.*107+53660_*107+53661insTTCTTG
ENST00000706494.1:c.-60+53660_-60+53661insTTCTTG (FGF14)	ENSP00000516417.1:n.-60+53660_-60+53661insTTCTTG
ENST00000376131.8:c.208+88686_208+88687insTTCTTG (FGF14)	ENSP00000365301.3:n.208+88686_208+88687insTTCTTG
NM_175929.2:c.208+88686_208+88687insTTCTTG (FGF14)	NP_787125.1:n.208+88686_208+88687insTTCTTG
NR_036486.1:n.410-18745_410-18744insTTCTTG (FGF14-IT1)
NM_001321935.1:c.-60+4851_-60+4852insTTCTTG (FGF14)	NP_001308864.1:n.-60+4851_-60+4852insTTCTTG
NM_001321936.1:c.-324+4851_-324+4852insTTCTTG (FGF14)	NP_001308865.1:n.-324+4851_-324+4852insTTCTTG
NM_001321937.1:c.208+88686_208+88687insTTCTTG (FGF14)	NP_001308866.1:n.208+88686_208+88687insTTCTTG
NM_001321938.1:c.-225+88686_-225+88687insTTCTTG (FGF14)	NP_001308867.1:n.-225+88686_-225+88687insTTCTTG
NM_001321939.1:c.208+88686_208+88687insTTCTTG (FGF14)	NP_001308868.1:n.208+88686_208+88687insTTCTTG
NM_001321940.1:c.-225+88686_-225+88687insTTCTTG (FGF14)	NP_001308869.1:n.-225+88686_-225+88687insTTCTTG
NM_001321941.1:c.-60-18745_-60-18744insTTCTTG (FGF14)	NP_001308870.1:n.-60-18745_-60-18744insTTCTTG
NM_001321942.1:c.-60+80973_-60+80974insTTCTTG (FGF14)	NP_001308871.1:n.-60+80973_-60+80974insTTCTTG
NM_001321943.1:c.-171+88686_-171+88687insTTCTTG (FGF14)	NP_001308872.1:n.-171+88686_-171+88687insTTCTTG
NM_001321944.1:c.-324+88686_-324+88687insTTCTTG (FGF14)	NP_001308873.1:n.-324+88686_-324+88687insTTCTTG
NM_001321945.1:c.91+88686_91+88687insTTCTTG (FGF14)	NP_001308874.1:n.91+88686_91+88687insTTCTTG
NM_001321946.1:c.-60+53660_-60+53661insTTCTTG (FGF14)	NP_001308875.1:n.-60+53660_-60+53661insTTCTTG
NM_001321947.1:c.52+88686_52+88687insTTCTTG (FGF14)	NP_001308876.1:n.52+88686_52+88687insTTCTTG
NM_001321948.1:c.91+88686_91+88687insTTCTTG (FGF14)	NP_001308877.1:n.91+88686_91+88687insTTCTTG
NM_001321949.1:c.-60+53660_-60+53661insTTCTTG (FGF14)	NP_001308878.1:n.-60+53660_-60+53661insTTCTTG
XR_001750081.2:n.6289_6290insCAAGAA
NM_001321938.2:c.-225+88686_-225+88687insTTCTTG (FGF14)	NP_001308867.1:n.-225+88686_-225+88687insTTCTTG
NM_001321945.2:c.91+88686_91+88687insTTCTTG (FGF14)	NP_001308874.1:n.91+88686_91+88687insTTCTTG
NM_001321946.2:c.-60+53660_-60+53661insTTCTTG (FGF14)	NP_001308875.1:n.-60+53660_-60+53661insTTCTTG
NM_001321947.2:c.52+88686_52+88687insTTCTTG (FGF14)	NP_001308876.1:n.52+88686_52+88687insTTCTTG
NM_001321948.2:c.91+88686_91+88687insTTCTTG (FGF14)	NP_001308877.1:n.91+88686_91+88687insTTCTTG
NM_001321937.2:c.208+88686_208+88687insTTCTTG (FGF14)	NP_001308866.1:n.208+88686_208+88687insTTCTTG
NM_001321939.2:c.208+88686_208+88687insTTCTTG (FGF14)	NP_001308868.1:n.208+88686_208+88687insTTCTTG
NM_001321941.2:c.-60-18745_-60-18744insTTCTTG (FGF14)	NP_001308870.1:n.-60-18745_-60-18744insTTCTTG
NM_001379342.1:c.91+88686_91+88687insTTCTTG (FGF14)	NP_001366271.1:n.91+88686_91+88687insTTCTTG
NM_175929.3:c.208+88686_208+88687insTTCTTG (FGF14)	NP_787125.1:n.208+88686_208+88687insTTCTTG