Canonical Allele Identifier: CA694333648

Gene: FGF14 FGF14-IT1

Linked Data

• dbSNP Id: rs1267402790
• gnomAD v3: 13-102312208-T-TG
• gnomAD v4: 13-102312208-T-TG
• MyVariant Identifiers: chr13:g.102964558_102964559insG (hg19) ; chr13:g.102312208_102312209insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312208_102312209insG , CM000675.2:g.102312208_102312209insG	GRCh38
NC_000013.10:g.102964558_102964559insG , CM000675.1:g.102964558_102964559insG	GRCh37
NC_000013.9:g.101762559_101762560insG	NCBI36
NG_008317.1:g.94566_94567insC
NG_008317.2:g.94566_94567insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+89262_208+89263insC (FGF14)	ENSP00000365301.3:n.208+89262_208+89263insC
ENST00000418923.3:c.91+89262_91+89263insC (FGF14)	ENSP00000516414.1:n.91+89262_91+89263insC
ENST00000706491.1:c.208+89262_208+89263insC (FGF14)	ENSP00000516413.1:n.208+89262_208+89263insC
ENST00000706492.1:c.*12+81549_*12+81550insC (FGF14)	ENSP00000516415.1:n.*12+81549_*12+81550insC
ENST00000706493.1:c.*107+54236_*107+54237insC (FGF14)	ENSP00000516416.1:n.*107+54236_*107+54237insC
ENST00000706494.1:c.-60+54236_-60+54237insC (FGF14)	ENSP00000516417.1:n.-60+54236_-60+54237insC
ENST00000376131.8:c.208+89262_208+89263insC (FGF14)	ENSP00000365301.3:n.208+89262_208+89263insC
NM_175929.2:c.208+89262_208+89263insC (FGF14)	NP_787125.1:n.208+89262_208+89263insC
NR_036486.1:n.410-18169_410-18168insC (FGF14-IT1)
NM_001321935.1:c.-60+5427_-60+5428insC (FGF14)	NP_001308864.1:n.-60+5427_-60+5428insC
NM_001321936.1:c.-324+5427_-324+5428insC (FGF14)	NP_001308865.1:n.-324+5427_-324+5428insC
NM_001321937.1:c.208+89262_208+89263insC (FGF14)	NP_001308866.1:n.208+89262_208+89263insC
NM_001321938.1:c.-225+89262_-225+89263insC (FGF14)	NP_001308867.1:n.-225+89262_-225+89263insC
NM_001321939.1:c.208+89262_208+89263insC (FGF14)	NP_001308868.1:n.208+89262_208+89263insC
NM_001321940.1:c.-225+89262_-225+89263insC (FGF14)	NP_001308869.1:n.-225+89262_-225+89263insC
NM_001321941.1:c.-60-18169_-60-18168insC (FGF14)	NP_001308870.1:n.-60-18169_-60-18168insC
NM_001321942.1:c.-60+81549_-60+81550insC (FGF14)	NP_001308871.1:n.-60+81549_-60+81550insC
NM_001321943.1:c.-171+89262_-171+89263insC (FGF14)	NP_001308872.1:n.-171+89262_-171+89263insC
NM_001321944.1:c.-324+89262_-324+89263insC (FGF14)	NP_001308873.1:n.-324+89262_-324+89263insC
NM_001321945.1:c.91+89262_91+89263insC (FGF14)	NP_001308874.1:n.91+89262_91+89263insC
NM_001321946.1:c.-60+54236_-60+54237insC (FGF14)	NP_001308875.1:n.-60+54236_-60+54237insC
NM_001321947.1:c.52+89262_52+89263insC (FGF14)	NP_001308876.1:n.52+89262_52+89263insC
NM_001321948.1:c.91+89262_91+89263insC (FGF14)	NP_001308877.1:n.91+89262_91+89263insC
NM_001321949.1:c.-60+54236_-60+54237insC (FGF14)	NP_001308878.1:n.-60+54236_-60+54237insC
XR_001750081.2:n.6248-535_6248-534insG
NM_001321938.2:c.-225+89262_-225+89263insC (FGF14)	NP_001308867.1:n.-225+89262_-225+89263insC
NM_001321945.2:c.91+89262_91+89263insC (FGF14)	NP_001308874.1:n.91+89262_91+89263insC
NM_001321946.2:c.-60+54236_-60+54237insC (FGF14)	NP_001308875.1:n.-60+54236_-60+54237insC
NM_001321947.2:c.52+89262_52+89263insC (FGF14)	NP_001308876.1:n.52+89262_52+89263insC
NM_001321948.2:c.91+89262_91+89263insC (FGF14)	NP_001308877.1:n.91+89262_91+89263insC
NM_001321937.2:c.208+89262_208+89263insC (FGF14)	NP_001308866.1:n.208+89262_208+89263insC
NM_001321939.2:c.208+89262_208+89263insC (FGF14)	NP_001308868.1:n.208+89262_208+89263insC
NM_001321941.2:c.-60-18169_-60-18168insC (FGF14)	NP_001308870.1:n.-60-18169_-60-18168insC
NM_001379342.1:c.91+89262_91+89263insC (FGF14)	NP_001366271.1:n.91+89262_91+89263insC
NM_175929.3:c.208+89262_208+89263insC (FGF14)	NP_787125.1:n.208+89262_208+89263insC