Canonical Allele Identifier: CA959615237

Gene: FGF14 FGF14-IT1

Linked Data

• dbSNP Id: rs2055849578
• gnomAD v3: 13-102313026-C-CCT
• gnomAD v4: 13-102313026-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102313027_102313028dup , CM000675.2:g.102313027_102313028dup	GRCh38
NC_000013.10:g.102965377_102965378dup , CM000675.1:g.102965377_102965378dup	GRCh37
NC_000013.9:g.101763378_101763379dup	NCBI36
NG_008317.1:g.93747_93748dup
NG_008317.2:g.93747_93748dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+88443_208+88444dup (FGF14)	ENSP00000365301.3:n.208+88443_208+88444dup
ENST00000418923.3:c.91+88443_91+88444dup (FGF14)	ENSP00000516414.1:n.91+88443_91+88444dup
ENST00000706491.1:c.208+88443_208+88444dup (FGF14)	ENSP00000516413.1:n.208+88443_208+88444dup
ENST00000706492.1:c.*12+80730_*12+80731dup (FGF14)	ENSP00000516415.1:n.*12+80730_*12+80731dup
ENST00000706493.1:c.*107+53417_*107+53418dup (FGF14)	ENSP00000516416.1:n.*107+53417_*107+53418dup
ENST00000706494.1:c.-60+53417_-60+53418dup (FGF14)	ENSP00000516417.1:n.-60+53417_-60+53418dup
ENST00000376131.8:c.208+88443_208+88444dup (FGF14)	ENSP00000365301.3:n.208+88443_208+88444dup
NM_175929.2:c.208+88443_208+88444dup (FGF14)	NP_787125.1:n.208+88443_208+88444dup
NR_036486.1:n.410-18988_410-18987dup (FGF14-IT1)
NM_001321935.1:c.-60+4608_-60+4609dup (FGF14)	NP_001308864.1:n.-60+4608_-60+4609dup
NM_001321936.1:c.-324+4608_-324+4609dup (FGF14)	NP_001308865.1:n.-324+4608_-324+4609dup
NM_001321937.1:c.208+88443_208+88444dup (FGF14)	NP_001308866.1:n.208+88443_208+88444dup
NM_001321938.1:c.-225+88443_-225+88444dup (FGF14)	NP_001308867.1:n.-225+88443_-225+88444dup
NM_001321939.1:c.208+88443_208+88444dup (FGF14)	NP_001308868.1:n.208+88443_208+88444dup
NM_001321940.1:c.-225+88443_-225+88444dup (FGF14)	NP_001308869.1:n.-225+88443_-225+88444dup
NM_001321941.1:c.-60-18988_-60-18987dup (FGF14)	NP_001308870.1:n.-60-18988_-60-18987dup
NM_001321942.1:c.-60+80730_-60+80731dup (FGF14)	NP_001308871.1:n.-60+80730_-60+80731dup
NM_001321943.1:c.-171+88443_-171+88444dup (FGF14)	NP_001308872.1:n.-171+88443_-171+88444dup
NM_001321944.1:c.-324+88443_-324+88444dup (FGF14)	NP_001308873.1:n.-324+88443_-324+88444dup
NM_001321945.1:c.91+88443_91+88444dup (FGF14)	NP_001308874.1:n.91+88443_91+88444dup
NM_001321946.1:c.-60+53417_-60+53418dup (FGF14)	NP_001308875.1:n.-60+53417_-60+53418dup
NM_001321947.1:c.52+88443_52+88444dup (FGF14)	NP_001308876.1:n.52+88443_52+88444dup
NM_001321948.1:c.91+88443_91+88444dup (FGF14)	NP_001308877.1:n.91+88443_91+88444dup
NM_001321949.1:c.-60+53417_-60+53418dup (FGF14)	NP_001308878.1:n.-60+53417_-60+53418dup
NM_001321938.2:c.-225+88443_-225+88444dup (FGF14)	NP_001308867.1:n.-225+88443_-225+88444dup
NM_001321945.2:c.91+88443_91+88444dup (FGF14)	NP_001308874.1:n.91+88443_91+88444dup
NM_001321946.2:c.-60+53417_-60+53418dup (FGF14)	NP_001308875.1:n.-60+53417_-60+53418dup
NM_001321947.2:c.52+88443_52+88444dup (FGF14)	NP_001308876.1:n.52+88443_52+88444dup
NM_001321948.2:c.91+88443_91+88444dup (FGF14)	NP_001308877.1:n.91+88443_91+88444dup
NM_001321937.2:c.208+88443_208+88444dup (FGF14)	NP_001308866.1:n.208+88443_208+88444dup
NM_001321939.2:c.208+88443_208+88444dup (FGF14)	NP_001308868.1:n.208+88443_208+88444dup
NM_001321941.2:c.-60-18988_-60-18987dup (FGF14)	NP_001308870.1:n.-60-18988_-60-18987dup
NM_001379342.1:c.91+88443_91+88444dup (FGF14)	NP_001366271.1:n.91+88443_91+88444dup
NM_175929.3:c.208+88443_208+88444dup (FGF14)	NP_787125.1:n.208+88443_208+88444dup