Canonical Allele Identifier: CA484767619

Gene: FGF14

Linked Data

• dbSNP Id: rs1339550466
• gnomAD v2: 13-102379113-A-G
• gnomAD v4: 13-101726763-A-G
• MyVariant Identifiers: chr13:g.102379113A>G (hg19) ; chr13:g.101726763A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726763A>G , CM000675.2:g.101726763A>G	GRCh38
NC_000013.10:g.102379113A>G , CM000675.1:g.102379113A>G	GRCh37
NC_000013.9:g.101177114A>G	NCBI36
NG_008317.1:g.680012T>C
NG_008317.2:g.680012T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.471T>C	ENSP00000365301.3:p.Asn157=
ENST00000418923.3:c.354T>C	ENSP00000516414.1:p.Asn118=
ENST00000706491.1:c.*60T>C	ENSP00000516413.1:n.*60T>C
ENST00000706492.1:c.*275T>C	ENSP00000516415.1:n.*275T>C
ENST00000706493.1:c.*370T>C	ENSP00000516416.1:n.*370T>C
ENST00000706494.1:c.204T>C	ENSP00000516417.1:p.Asn68=
ENST00000376143.5:c.456T>C MANE Select	ENSP00000365313.4:p.Asn152=
ENST00000376131.8:c.471T>C	ENSP00000365301.3:p.Asn157=
ENST00000376143.4:c.456T>C	ENSP00000365313.4:p.Asn152=
NM_004115.3:c.456T>C	NP_004106.1:p.Asn152=
NM_175929.2:c.471T>C	NP_787125.1:p.Asn157=
XM_011521053.1:c.276T>C	XP_011519355.1:p.Asn92=
NM_001321931.1:c.204T>C	NP_001308860.1:p.Asn68=
NM_001321932.1:c.267T>C	NP_001308861.1:p.Asn89=
NM_001321933.1:c.276T>C	NP_001308862.1:p.Asn92=
NM_001321934.1:c.204T>C	NP_001308863.1:p.Asn68=
NM_001321935.1:c.204T>C	NP_001308864.1:p.Asn68=
NM_001321936.1:c.267T>C	NP_001308865.1:p.Asn89=
NM_001321938.1:c.276T>C	NP_001308867.1:p.Asn92=
NM_001321939.1:c.360T>C	NP_001308868.1:p.Asn120=
NM_001321940.1:c.276T>C	NP_001308869.1:p.Asn92=
NM_001321941.1:c.270T>C	NP_001308870.1:p.Asn90=
NM_001321942.1:c.204T>C	NP_001308871.1:p.Asn68=
NM_001321943.1:c.204T>C	NP_001308872.1:p.Asn68=
NM_001321944.1:c.267T>C	NP_001308873.1:p.Asn89=
NM_001321945.1:c.354T>C	NP_001308874.1:p.Asn118=
NM_001321946.1:c.204T>C	NP_001308875.1:p.Asn68=
NM_001321947.1:c.315T>C	NP_001308876.1:p.Asn105=
NM_001321948.1:c.354T>C	NP_001308877.1:p.Asn118=
NM_001321949.1:c.204T>C	NP_001308878.1:p.Asn68=
NM_001321938.2:c.276T>C	NP_001308867.1:p.Asn92=
NM_001321945.2:c.354T>C	NP_001308874.1:p.Asn118=
NM_001321946.2:c.204T>C	NP_001308875.1:p.Asn68=
NM_001321947.2:c.315T>C	NP_001308876.1:p.Asn105=
NM_001321948.2:c.354T>C	NP_001308877.1:p.Asn118=
NM_001321939.2:c.360T>C	NP_001308868.1:p.Asn120=
NM_001321941.2:c.270T>C	NP_001308870.1:p.Asn90=
NM_001379342.1:c.354T>C	NP_001366271.1:p.Asn118=
NM_004115.4:c.456T>C MANE Select	NP_004106.1:p.Asn152=
NM_175929.3:c.471T>C	NP_787125.1:p.Asn157=