Canonical Allele Identifier: CA959614739

Gene: FGF14 FGF14-IT1

Linked Data

• dbSNP Id: rs2055806206
• gnomAD v3: 13-102312221-C-CAA
• gnomAD v4: 13-102312221-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312221_102312222insAA , CM000675.2:g.102312221_102312222insAA	GRCh38
NC_000013.10:g.102964571_102964572insAA , CM000675.1:g.102964571_102964572insAA	GRCh37
NC_000013.9:g.101762572_101762573insAA	NCBI36
NG_008317.1:g.94553_94554insTT
NG_008317.2:g.94553_94554insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+89249_208+89250insTT (FGF14)	ENSP00000365301.3:n.208+89249_208+89250insTT
ENST00000418923.3:c.91+89249_91+89250insTT (FGF14)	ENSP00000516414.1:n.91+89249_91+89250insTT
ENST00000706491.1:c.208+89249_208+89250insTT (FGF14)	ENSP00000516413.1:n.208+89249_208+89250insTT
ENST00000706492.1:c.*12+81536_*12+81537insTT (FGF14)	ENSP00000516415.1:n.*12+81536_*12+81537insTT
ENST00000706493.1:c.*107+54223_*107+54224insTT (FGF14)	ENSP00000516416.1:n.*107+54223_*107+54224insTT
ENST00000706494.1:c.-60+54223_-60+54224insTT (FGF14)	ENSP00000516417.1:n.-60+54223_-60+54224insTT
ENST00000376131.8:c.208+89249_208+89250insTT (FGF14)	ENSP00000365301.3:n.208+89249_208+89250insTT
NM_175929.2:c.208+89249_208+89250insTT (FGF14)	NP_787125.1:n.208+89249_208+89250insTT
NR_036486.1:n.410-18182_410-18181insTT (FGF14-IT1)
NM_001321935.1:c.-60+5414_-60+5415insTT (FGF14)	NP_001308864.1:n.-60+5414_-60+5415insTT
NM_001321936.1:c.-324+5414_-324+5415insTT (FGF14)	NP_001308865.1:n.-324+5414_-324+5415insTT
NM_001321937.1:c.208+89249_208+89250insTT (FGF14)	NP_001308866.1:n.208+89249_208+89250insTT
NM_001321938.1:c.-225+89249_-225+89250insTT (FGF14)	NP_001308867.1:n.-225+89249_-225+89250insTT
NM_001321939.1:c.208+89249_208+89250insTT (FGF14)	NP_001308868.1:n.208+89249_208+89250insTT
NM_001321940.1:c.-225+89249_-225+89250insTT (FGF14)	NP_001308869.1:n.-225+89249_-225+89250insTT
NM_001321941.1:c.-60-18182_-60-18181insTT (FGF14)	NP_001308870.1:n.-60-18182_-60-18181insTT
NM_001321942.1:c.-60+81536_-60+81537insTT (FGF14)	NP_001308871.1:n.-60+81536_-60+81537insTT
NM_001321943.1:c.-171+89249_-171+89250insTT (FGF14)	NP_001308872.1:n.-171+89249_-171+89250insTT
NM_001321944.1:c.-324+89249_-324+89250insTT (FGF14)	NP_001308873.1:n.-324+89249_-324+89250insTT
NM_001321945.1:c.91+89249_91+89250insTT (FGF14)	NP_001308874.1:n.91+89249_91+89250insTT
NM_001321946.1:c.-60+54223_-60+54224insTT (FGF14)	NP_001308875.1:n.-60+54223_-60+54224insTT
NM_001321947.1:c.52+89249_52+89250insTT (FGF14)	NP_001308876.1:n.52+89249_52+89250insTT
NM_001321948.1:c.91+89249_91+89250insTT (FGF14)	NP_001308877.1:n.91+89249_91+89250insTT
NM_001321949.1:c.-60+54223_-60+54224insTT (FGF14)	NP_001308878.1:n.-60+54223_-60+54224insTT
XR_001750081.2:n.6248-522_6248-521insAA
NM_001321938.2:c.-225+89249_-225+89250insTT (FGF14)	NP_001308867.1:n.-225+89249_-225+89250insTT
NM_001321945.2:c.91+89249_91+89250insTT (FGF14)	NP_001308874.1:n.91+89249_91+89250insTT
NM_001321946.2:c.-60+54223_-60+54224insTT (FGF14)	NP_001308875.1:n.-60+54223_-60+54224insTT
NM_001321947.2:c.52+89249_52+89250insTT (FGF14)	NP_001308876.1:n.52+89249_52+89250insTT
NM_001321948.2:c.91+89249_91+89250insTT (FGF14)	NP_001308877.1:n.91+89249_91+89250insTT
NM_001321937.2:c.208+89249_208+89250insTT (FGF14)	NP_001308866.1:n.208+89249_208+89250insTT
NM_001321939.2:c.208+89249_208+89250insTT (FGF14)	NP_001308868.1:n.208+89249_208+89250insTT
NM_001321941.2:c.-60-18182_-60-18181insTT (FGF14)	NP_001308870.1:n.-60-18182_-60-18181insTT
NM_001379342.1:c.91+89249_91+89250insTT (FGF14)	NP_001366271.1:n.91+89249_91+89250insTT
NM_175929.3:c.208+89249_208+89250insTT (FGF14)	NP_787125.1:n.208+89249_208+89250insTT