Canonical Allele Identifier: CA388711272

Gene: FGF14

Linked Data

• dbSNP Id: rs1566823396
• MyVariant Identifiers: chr13:g.102379090A>G (hg19) ; chr13:g.101726740A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101726740A>G , CM000675.2:g.101726740A>G	GRCh38
NC_000013.10:g.102379090A>G , CM000675.1:g.102379090A>G	GRCh37
NC_000013.9:g.101177091A>G	NCBI36
NG_008317.1:g.680035T>C
NG_008317.2:g.680035T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376131.9:c.494T>C	ENSP00000365301.3:p.Met165Thr
ENST00000418923.3:c.377T>C	ENSP00000516414.1:p.Met126Thr
ENST00000706491.1:c.*83T>C	ENSP00000516413.1:n.*83T>C
ENST00000706492.1:c.*298T>C	ENSP00000516415.1:n.*298T>C
ENST00000706493.1:c.*393T>C	ENSP00000516416.1:n.*393T>C
ENST00000706494.1:c.227T>C	ENSP00000516417.1:p.Met76Thr
ENST00000376143.5:c.479T>C MANE Select	ENSP00000365313.4:p.Met160Thr
ENST00000376131.8:c.494T>C	ENSP00000365301.3:p.Met165Thr
ENST00000376143.4:c.479T>C	ENSP00000365313.4:p.Met160Thr
NM_004115.3:c.479T>C	NP_004106.1:p.Met160Thr
NM_175929.2:c.494T>C	NP_787125.1:p.Met165Thr
XM_011521053.1:c.299T>C	XP_011519355.1:p.Met100Thr
NM_001321931.1:c.227T>C	NP_001308860.1:p.Met76Thr
NM_001321932.1:c.290T>C	NP_001308861.1:p.Met97Thr
NM_001321933.1:c.299T>C	NP_001308862.1:p.Met100Thr
NM_001321934.1:c.227T>C	NP_001308863.1:p.Met76Thr
NM_001321935.1:c.227T>C	NP_001308864.1:p.Met76Thr
NM_001321936.1:c.290T>C	NP_001308865.1:p.Met97Thr
NM_001321938.1:c.299T>C	NP_001308867.1:p.Met100Thr
NM_001321939.1:c.383T>C	NP_001308868.1:p.Met128Thr
NM_001321940.1:c.299T>C	NP_001308869.1:p.Met100Thr
NM_001321941.1:c.293T>C	NP_001308870.1:p.Met98Thr
NM_001321942.1:c.227T>C	NP_001308871.1:p.Met76Thr
NM_001321943.1:c.227T>C	NP_001308872.1:p.Met76Thr
NM_001321944.1:c.290T>C	NP_001308873.1:p.Met97Thr
NM_001321945.1:c.377T>C	NP_001308874.1:p.Met126Thr
NM_001321946.1:c.227T>C	NP_001308875.1:p.Met76Thr
NM_001321947.1:c.338T>C	NP_001308876.1:p.Met113Thr
NM_001321948.1:c.377T>C	NP_001308877.1:p.Met126Thr
NM_001321949.1:c.227T>C	NP_001308878.1:p.Met76Thr
NM_001321938.2:c.299T>C	NP_001308867.1:p.Met100Thr
NM_001321945.2:c.377T>C	NP_001308874.1:p.Met126Thr
NM_001321946.2:c.227T>C	NP_001308875.1:p.Met76Thr
NM_001321947.2:c.338T>C	NP_001308876.1:p.Met113Thr
NM_001321948.2:c.377T>C	NP_001308877.1:p.Met126Thr
NM_001321939.2:c.383T>C	NP_001308868.1:p.Met128Thr
NM_001321941.2:c.293T>C	NP_001308870.1:p.Met98Thr
NM_001379342.1:c.377T>C	NP_001366271.1:p.Met126Thr
NM_004115.4:c.479T>C MANE Select	NP_004106.1:p.Met160Thr
NM_175929.3:c.494T>C	NP_787125.1:p.Met165Thr