Canonical Allele Identifier: CA959614661

Gene: FGF14 FGF14-IT1

Linked Data

• gnomAD v3: 13-102312206-AGT-A
• gnomAD v4: 13-102312206-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312207_102312208del , CM000675.2:g.102312207_102312208del	GRCh38
NC_000013.10:g.102964557_102964558del , CM000675.1:g.102964557_102964558del	GRCh37
NC_000013.9:g.101762558_101762559del	NCBI36
NG_008317.1:g.94567_94568del
NG_008317.2:g.94567_94568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+89263_208+89264del (FGF14)	ENSP00000365301.3:n.208+89263_208+89264del
ENST00000418923.3:c.91+89263_91+89264del (FGF14)	ENSP00000516414.1:n.91+89263_91+89264del
ENST00000706491.1:c.208+89263_208+89264del (FGF14)	ENSP00000516413.1:n.208+89263_208+89264del
ENST00000706492.1:c.*12+81550_*12+81551del (FGF14)	ENSP00000516415.1:n.*12+81550_*12+81551del
ENST00000706493.1:c.*107+54237_*107+54238del (FGF14)	ENSP00000516416.1:n.*107+54237_*107+54238del
ENST00000706494.1:c.-60+54237_-60+54238del (FGF14)	ENSP00000516417.1:n.-60+54237_-60+54238del
ENST00000376131.8:c.208+89263_208+89264del (FGF14)	ENSP00000365301.3:n.208+89263_208+89264del
NM_175929.2:c.208+89263_208+89264del (FGF14)	NP_787125.1:n.208+89263_208+89264del
NR_036486.1:n.410-18168_410-18167del (FGF14-IT1)
NM_001321935.1:c.-60+5428_-60+5429del (FGF14)	NP_001308864.1:n.-60+5428_-60+5429del
NM_001321936.1:c.-324+5428_-324+5429del (FGF14)	NP_001308865.1:n.-324+5428_-324+5429del
NM_001321937.1:c.208+89263_208+89264del (FGF14)	NP_001308866.1:n.208+89263_208+89264del
NM_001321938.1:c.-225+89263_-225+89264del (FGF14)	NP_001308867.1:n.-225+89263_-225+89264del
NM_001321939.1:c.208+89263_208+89264del (FGF14)	NP_001308868.1:n.208+89263_208+89264del
NM_001321940.1:c.-225+89263_-225+89264del (FGF14)	NP_001308869.1:n.-225+89263_-225+89264del
NM_001321941.1:c.-60-18168_-60-18167del (FGF14)	NP_001308870.1:n.-60-18168_-60-18167del
NM_001321942.1:c.-60+81550_-60+81551del (FGF14)	NP_001308871.1:n.-60+81550_-60+81551del
NM_001321943.1:c.-171+89263_-171+89264del (FGF14)	NP_001308872.1:n.-171+89263_-171+89264del
NM_001321944.1:c.-324+89263_-324+89264del (FGF14)	NP_001308873.1:n.-324+89263_-324+89264del
NM_001321945.1:c.91+89263_91+89264del (FGF14)	NP_001308874.1:n.91+89263_91+89264del
NM_001321946.1:c.-60+54237_-60+54238del (FGF14)	NP_001308875.1:n.-60+54237_-60+54238del
NM_001321947.1:c.52+89263_52+89264del (FGF14)	NP_001308876.1:n.52+89263_52+89264del
NM_001321948.1:c.91+89263_91+89264del (FGF14)	NP_001308877.1:n.91+89263_91+89264del
NM_001321949.1:c.-60+54237_-60+54238del (FGF14)	NP_001308878.1:n.-60+54237_-60+54238del
XR_001750081.2:n.6248-536_6248-535del
NM_001321938.2:c.-225+89263_-225+89264del (FGF14)	NP_001308867.1:n.-225+89263_-225+89264del
NM_001321945.2:c.91+89263_91+89264del (FGF14)	NP_001308874.1:n.91+89263_91+89264del
NM_001321946.2:c.-60+54237_-60+54238del (FGF14)	NP_001308875.1:n.-60+54237_-60+54238del
NM_001321947.2:c.52+89263_52+89264del (FGF14)	NP_001308876.1:n.52+89263_52+89264del
NM_001321948.2:c.91+89263_91+89264del (FGF14)	NP_001308877.1:n.91+89263_91+89264del
NM_001321937.2:c.208+89263_208+89264del (FGF14)	NP_001308866.1:n.208+89263_208+89264del
NM_001321939.2:c.208+89263_208+89264del (FGF14)	NP_001308868.1:n.208+89263_208+89264del
NM_001321941.2:c.-60-18168_-60-18167del (FGF14)	NP_001308870.1:n.-60-18168_-60-18167del
NM_001379342.1:c.91+89263_91+89264del (FGF14)	NP_001366271.1:n.91+89263_91+89264del
NM_175929.3:c.208+89263_208+89264del (FGF14)	NP_787125.1:n.208+89263_208+89264del