Canonical Allele Identifier: CA2623591693

Gene: FGF14

Linked Data

• gnomAD v4: 13-101726771-A-ATTG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726771_101726772insTTG , CM000675.2:g.101726771_101726772insTTG	GRCh38
NC_000013.10:g.102379121_102379122insTTG , CM000675.1:g.102379121_102379122insTTG	GRCh37
NC_000013.9:g.101177122_101177123insTTG	NCBI36
NG_008317.1:g.680003_680004insCAA
NG_008317.2:g.680003_680004insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.462_463insCAA	ENSP00000365301.3:p.Val154_Phe155insGln
ENST00000418923.3:c.345_346insCAA	ENSP00000516414.1:p.Val115_Phe116insGln
ENST00000706491.1:c.*51_*52insCAA	ENSP00000516413.1:n.*51_*52insCAA
ENST00000706492.1:c.*266_*267insCAA	ENSP00000516415.1:n.*266_*267insCAA
ENST00000706493.1:c.*361_*362insCAA	ENSP00000516416.1:n.*361_*362insCAA
ENST00000706494.1:c.195_196insCAA	ENSP00000516417.1:p.Val65_Phe66insGln
ENST00000376143.5:c.447_448insCAA MANE Select	ENSP00000365313.4:p.Val149_Phe150insGln
ENST00000376131.8:c.462_463insCAA	ENSP00000365301.3:p.Val154_Phe155insGln
ENST00000376143.4:c.447_448insCAA	ENSP00000365313.4:p.Val149_Phe150insGln
NM_004115.3:c.447_448insCAA	NP_004106.1:p.Val149_Phe150insGln
NM_175929.2:c.462_463insCAA	NP_787125.1:p.Val154_Phe155insGln
XM_011521053.1:c.267_268insCAA	XP_011519355.1:p.Val89_Phe90insGln
NM_001321931.1:c.195_196insCAA	NP_001308860.1:p.Val65_Phe66insGln
NM_001321932.1:c.258_259insCAA	NP_001308861.1:p.Val86_Phe87insGln
NM_001321933.1:c.267_268insCAA	NP_001308862.1:p.Val89_Phe90insGln
NM_001321934.1:c.195_196insCAA	NP_001308863.1:p.Val65_Phe66insGln
NM_001321935.1:c.195_196insCAA	NP_001308864.1:p.Val65_Phe66insGln
NM_001321936.1:c.258_259insCAA	NP_001308865.1:p.Val86_Phe87insGln
NM_001321938.1:c.267_268insCAA	NP_001308867.1:p.Val89_Phe90insGln
NM_001321939.1:c.351_352insCAA	NP_001308868.1:p.Val117_Phe118insGln
NM_001321940.1:c.267_268insCAA	NP_001308869.1:p.Val89_Phe90insGln
NM_001321941.1:c.261_262insCAA	NP_001308870.1:p.Val87_Phe88insGln
NM_001321942.1:c.195_196insCAA	NP_001308871.1:p.Val65_Phe66insGln
NM_001321943.1:c.195_196insCAA	NP_001308872.1:p.Val65_Phe66insGln
NM_001321944.1:c.258_259insCAA	NP_001308873.1:p.Val86_Phe87insGln
NM_001321945.1:c.345_346insCAA	NP_001308874.1:p.Val115_Phe116insGln
NM_001321946.1:c.195_196insCAA	NP_001308875.1:p.Val65_Phe66insGln
NM_001321947.1:c.306_307insCAA	NP_001308876.1:p.Val102_Phe103insGln
NM_001321948.1:c.345_346insCAA	NP_001308877.1:p.Val115_Phe116insGln
NM_001321949.1:c.195_196insCAA	NP_001308878.1:p.Val65_Phe66insGln
NM_001321938.2:c.267_268insCAA	NP_001308867.1:p.Val89_Phe90insGln
NM_001321945.2:c.345_346insCAA	NP_001308874.1:p.Val115_Phe116insGln
NM_001321946.2:c.195_196insCAA	NP_001308875.1:p.Val65_Phe66insGln
NM_001321947.2:c.306_307insCAA	NP_001308876.1:p.Val102_Phe103insGln
NM_001321948.2:c.345_346insCAA	NP_001308877.1:p.Val115_Phe116insGln
NM_001321939.2:c.351_352insCAA	NP_001308868.1:p.Val117_Phe118insGln
NM_001321941.2:c.261_262insCAA	NP_001308870.1:p.Val87_Phe88insGln
NM_001379342.1:c.345_346insCAA	NP_001366271.1:p.Val115_Phe116insGln
NM_004115.4:c.447_448insCAA MANE Select	NP_004106.1:p.Val149_Phe150insGln
NM_175929.3:c.462_463insCAA	NP_787125.1:p.Val154_Phe155insGln