Canonical Allele Identifier: CA959614774

Gene: FGF14 FGF14-IT1

Linked Data

• dbSNP Id: rs34575465
• gnomAD v3: 13-102312222-CAAAA-C
• gnomAD v4: 13-102312222-CAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102312236_102312239del , CM000675.2:g.102312236_102312239del	GRCh38
NC_000013.10:g.102964586_102964589del , CM000675.1:g.102964586_102964589del	GRCh37
NC_000013.9:g.101762587_101762590del	NCBI36
NG_008317.1:g.94549_94552del
NG_008317.2:g.94549_94552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.208+89245_208+89248del (FGF14)	ENSP00000365301.3:n.208+89245_208+89248del
ENST00000418923.3:c.91+89245_91+89248del (FGF14)	ENSP00000516414.1:n.91+89245_91+89248del
ENST00000706491.1:c.208+89245_208+89248del (FGF14)	ENSP00000516413.1:n.208+89245_208+89248del
ENST00000706492.1:c.*12+81532_*12+81535del (FGF14)	ENSP00000516415.1:n.*12+81532_*12+81535del
ENST00000706493.1:c.*107+54219_*107+54222del (FGF14)	ENSP00000516416.1:n.*107+54219_*107+54222del
ENST00000706494.1:c.-60+54219_-60+54222del (FGF14)	ENSP00000516417.1:n.-60+54219_-60+54222del
ENST00000376131.8:c.208+89245_208+89248del (FGF14)	ENSP00000365301.3:n.208+89245_208+89248del
NM_175929.2:c.208+89245_208+89248del (FGF14)	NP_787125.1:n.208+89245_208+89248del
NR_036486.1:n.410-18186_410-18183del (FGF14-IT1)
NM_001321935.1:c.-60+5410_-60+5413del (FGF14)	NP_001308864.1:n.-60+5410_-60+5413del
NM_001321936.1:c.-324+5410_-324+5413del (FGF14)	NP_001308865.1:n.-324+5410_-324+5413del
NM_001321937.1:c.208+89245_208+89248del (FGF14)	NP_001308866.1:n.208+89245_208+89248del
NM_001321938.1:c.-225+89245_-225+89248del (FGF14)	NP_001308867.1:n.-225+89245_-225+89248del
NM_001321939.1:c.208+89245_208+89248del (FGF14)	NP_001308868.1:n.208+89245_208+89248del
NM_001321940.1:c.-225+89245_-225+89248del (FGF14)	NP_001308869.1:n.-225+89245_-225+89248del
NM_001321941.1:c.-60-18186_-60-18183del (FGF14)	NP_001308870.1:n.-60-18186_-60-18183del
NM_001321942.1:c.-60+81532_-60+81535del (FGF14)	NP_001308871.1:n.-60+81532_-60+81535del
NM_001321943.1:c.-171+89245_-171+89248del (FGF14)	NP_001308872.1:n.-171+89245_-171+89248del
NM_001321944.1:c.-324+89245_-324+89248del (FGF14)	NP_001308873.1:n.-324+89245_-324+89248del
NM_001321945.1:c.91+89245_91+89248del (FGF14)	NP_001308874.1:n.91+89245_91+89248del
NM_001321946.1:c.-60+54219_-60+54222del (FGF14)	NP_001308875.1:n.-60+54219_-60+54222del
NM_001321947.1:c.52+89245_52+89248del (FGF14)	NP_001308876.1:n.52+89245_52+89248del
NM_001321948.1:c.91+89245_91+89248del (FGF14)	NP_001308877.1:n.91+89245_91+89248del
NM_001321949.1:c.-60+54219_-60+54222del (FGF14)	NP_001308878.1:n.-60+54219_-60+54222del
XR_001750081.2:n.6248-507_6248-504del
NM_001321938.2:c.-225+89245_-225+89248del (FGF14)	NP_001308867.1:n.-225+89245_-225+89248del
NM_001321945.2:c.91+89245_91+89248del (FGF14)	NP_001308874.1:n.91+89245_91+89248del
NM_001321946.2:c.-60+54219_-60+54222del (FGF14)	NP_001308875.1:n.-60+54219_-60+54222del
NM_001321947.2:c.52+89245_52+89248del (FGF14)	NP_001308876.1:n.52+89245_52+89248del
NM_001321948.2:c.91+89245_91+89248del (FGF14)	NP_001308877.1:n.91+89245_91+89248del
NM_001321937.2:c.208+89245_208+89248del (FGF14)	NP_001308866.1:n.208+89245_208+89248del
NM_001321939.2:c.208+89245_208+89248del (FGF14)	NP_001308868.1:n.208+89245_208+89248del
NM_001321941.2:c.-60-18186_-60-18183del (FGF14)	NP_001308870.1:n.-60-18186_-60-18183del
NM_001379342.1:c.91+89245_91+89248del (FGF14)	NP_001366271.1:n.91+89245_91+89248del
NM_175929.3:c.208+89245_208+89248del (FGF14)	NP_787125.1:n.208+89245_208+89248del