Canonical Allele Identifier: CA2580087033

Gene: FGF14

Linked Data

• ClinVar Variation Id: 2300494
• ClinVar RCV Id: RCV002882919

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726757_101728057del , CM000675.2:g.101726757_101728057del	GRCh38
NC_000013.10:g.102379107_102380407del , CM000675.1:g.102379107_102380407del	GRCh37
NC_000013.9:g.101177108_101178408del	NCBI36
NG_008317.1:g.678720_680020del
NG_008317.2:g.678720_680020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.424-1245_479del
ENST00000418923.3:c.307-1245_362del
ENST00000706491.1:c.*13-1245_*68del
ENST00000706492.1:c.*228-1245_*283del
ENST00000706493.1:c.*323-1245_*378del
ENST00000706494.1:c.157-1245_212del
ENST00000376143.5:c.409-1245_464del
ENST00000376131.8:c.424-1245_479del
ENST00000376143.4:c.409-1245_464del
NM_004115.3:c.409-1245_464del
NM_175929.2:c.424-1245_479del
XM_011521053.1:c.229-1245_284del
NM_001321931.1:c.157-1245_212del
NM_001321932.1:c.220-1245_275del
NM_001321933.1:c.229-1245_284del
NM_001321934.1:c.157-1245_212del
NM_001321935.1:c.157-1245_212del
NM_001321936.1:c.220-1245_275del
NM_001321938.1:c.229-1245_284del
NM_001321939.1:c.313-1245_368del
NM_001321940.1:c.229-1245_284del
NM_001321941.1:c.223-1245_278del
NM_001321942.1:c.157-1245_212del
NM_001321943.1:c.157-1245_212del
NM_001321944.1:c.220-1245_275del
NM_001321945.1:c.307-1245_362del
NM_001321946.1:c.157-1245_212del
NM_001321947.1:c.268-1245_323del
NM_001321948.1:c.307-1245_362del
NM_001321949.1:c.157-1245_212del
NM_001321938.2:c.229-1245_284del
NM_001321945.2:c.307-1245_362del
NM_001321946.2:c.157-1245_212del
NM_001321947.2:c.268-1245_323del
NM_001321948.2:c.307-1245_362del
NM_001321939.2:c.313-1245_368del
NM_001321941.2:c.223-1245_278del
NM_001379342.1:c.307-1245_362del
NM_004115.4:c.409-1245_464del
NM_175929.3:c.424-1245_479del