Canonical Allele Identifier: CA959614890

Gene: FGF14 FGF14-IT1

Linked Data

• gnomAD v3: 13-102312242-C-CAAAA
• gnomAD v4: 13-102312242-C-CAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312245_102312246insAAAA , CM000675.2:g.102312245_102312246insAAAA	GRCh38
NC_000013.10:g.102964595_102964596insAAAA , CM000675.1:g.102964595_102964596insAAAA	GRCh37
NC_000013.9:g.101762596_101762597insAAAA	NCBI36
NG_008317.1:g.94532_94533insTTTT
NG_008317.2:g.94532_94533insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+89228_208+89229insTTTT (FGF14)	ENSP00000365301.3:n.208+89228_208+89229insTTTT
ENST00000418923.3:c.91+89228_91+89229insTTTT (FGF14)	ENSP00000516414.1:n.91+89228_91+89229insTTTT
ENST00000706491.1:c.208+89228_208+89229insTTTT (FGF14)	ENSP00000516413.1:n.208+89228_208+89229insTTTT
ENST00000706492.1:c.*12+81515_*12+81516insTTTT (FGF14)	ENSP00000516415.1:n.*12+81515_*12+81516insTTTT
ENST00000706493.1:c.*107+54202_*107+54203insTTTT (FGF14)	ENSP00000516416.1:n.*107+54202_*107+54203insTTTT
ENST00000706494.1:c.-60+54202_-60+54203insTTTT (FGF14)	ENSP00000516417.1:n.-60+54202_-60+54203insTTTT
ENST00000376131.8:c.208+89228_208+89229insTTTT (FGF14)	ENSP00000365301.3:n.208+89228_208+89229insTTTT
NM_175929.2:c.208+89228_208+89229insTTTT (FGF14)	NP_787125.1:n.208+89228_208+89229insTTTT
NR_036486.1:n.410-18203_410-18202insTTTT (FGF14-IT1)
NM_001321935.1:c.-60+5393_-60+5394insTTTT (FGF14)	NP_001308864.1:n.-60+5393_-60+5394insTTTT
NM_001321936.1:c.-324+5393_-324+5394insTTTT (FGF14)	NP_001308865.1:n.-324+5393_-324+5394insTTTT
NM_001321937.1:c.208+89228_208+89229insTTTT (FGF14)	NP_001308866.1:n.208+89228_208+89229insTTTT
NM_001321938.1:c.-225+89228_-225+89229insTTTT (FGF14)	NP_001308867.1:n.-225+89228_-225+89229insTTTT
NM_001321939.1:c.208+89228_208+89229insTTTT (FGF14)	NP_001308868.1:n.208+89228_208+89229insTTTT
NM_001321940.1:c.-225+89228_-225+89229insTTTT (FGF14)	NP_001308869.1:n.-225+89228_-225+89229insTTTT
NM_001321941.1:c.-60-18203_-60-18202insTTTT (FGF14)	NP_001308870.1:n.-60-18203_-60-18202insTTTT
NM_001321942.1:c.-60+81515_-60+81516insTTTT (FGF14)	NP_001308871.1:n.-60+81515_-60+81516insTTTT
NM_001321943.1:c.-171+89228_-171+89229insTTTT (FGF14)	NP_001308872.1:n.-171+89228_-171+89229insTTTT
NM_001321944.1:c.-324+89228_-324+89229insTTTT (FGF14)	NP_001308873.1:n.-324+89228_-324+89229insTTTT
NM_001321945.1:c.91+89228_91+89229insTTTT (FGF14)	NP_001308874.1:n.91+89228_91+89229insTTTT
NM_001321946.1:c.-60+54202_-60+54203insTTTT (FGF14)	NP_001308875.1:n.-60+54202_-60+54203insTTTT
NM_001321947.1:c.52+89228_52+89229insTTTT (FGF14)	NP_001308876.1:n.52+89228_52+89229insTTTT
NM_001321948.1:c.91+89228_91+89229insTTTT (FGF14)	NP_001308877.1:n.91+89228_91+89229insTTTT
NM_001321949.1:c.-60+54202_-60+54203insTTTT (FGF14)	NP_001308878.1:n.-60+54202_-60+54203insTTTT
XR_001750081.2:n.6248-498_6248-497insAAAA
NM_001321938.2:c.-225+89228_-225+89229insTTTT (FGF14)	NP_001308867.1:n.-225+89228_-225+89229insTTTT
NM_001321945.2:c.91+89228_91+89229insTTTT (FGF14)	NP_001308874.1:n.91+89228_91+89229insTTTT
NM_001321946.2:c.-60+54202_-60+54203insTTTT (FGF14)	NP_001308875.1:n.-60+54202_-60+54203insTTTT
NM_001321947.2:c.52+89228_52+89229insTTTT (FGF14)	NP_001308876.1:n.52+89228_52+89229insTTTT
NM_001321948.2:c.91+89228_91+89229insTTTT (FGF14)	NP_001308877.1:n.91+89228_91+89229insTTTT
NM_001321937.2:c.208+89228_208+89229insTTTT (FGF14)	NP_001308866.1:n.208+89228_208+89229insTTTT
NM_001321939.2:c.208+89228_208+89229insTTTT (FGF14)	NP_001308868.1:n.208+89228_208+89229insTTTT
NM_001321941.2:c.-60-18203_-60-18202insTTTT (FGF14)	NP_001308870.1:n.-60-18203_-60-18202insTTTT
NM_001379342.1:c.91+89228_91+89229insTTTT (FGF14)	NP_001366271.1:n.91+89228_91+89229insTTTT
NM_175929.3:c.208+89228_208+89229insTTTT (FGF14)	NP_787125.1:n.208+89228_208+89229insTTTT