Linked Data
dbSNP Id:
rs1566929188
gnomAD v2:
13-102964633-A-AG
gnomAD v3:
13-102312283-A-AG
gnomAD v4:
13-102312283-A-AG
MyVariant Identifiers:
chr13:g.102964633_102964634insG (hg19)
chr13:g.102312283_102312284insG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.102312283_102312284insG , CM000675.2:g.102312283_102312284insG | GRCh38 |
| NC_000013.10:g.102964633_102964634insG , CM000675.1:g.102964633_102964634insG | GRCh37 |
| NC_000013.9:g.101762634_101762635insG | NCBI36 |
| NG_008317.1:g.94491_94492insC | |
| NG_008317.2:g.94491_94492insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376131.9:c.208+89187_208+89188insC (FGF14) | ENSP00000365301.3:n.208+89187_208+89188insC | |
| ENST00000418923.3:c.91+89187_91+89188insC (FGF14) | ENSP00000516414.1:n.91+89187_91+89188insC | |
| ENST00000706491.1:c.208+89187_208+89188insC (FGF14) | ENSP00000516413.1:n.208+89187_208+89188insC | |
| ENST00000706492.1:c.*12+81474_*12+81475insC (FGF14) | ENSP00000516415.1:n.*12+81474_*12+81475insC | |
| ENST00000706493.1:c.*107+54161_*107+54162insC (FGF14) | ENSP00000516416.1:n.*107+54161_*107+54162insC | |
| ENST00000706494.1:c.-60+54161_-60+54162insC (FGF14) | ENSP00000516417.1:n.-60+54161_-60+54162insC | |
| ENST00000376131.8:c.208+89187_208+89188insC (FGF14) | ENSP00000365301.3:n.208+89187_208+89188insC | |
| NM_175929.2:c.208+89187_208+89188insC (FGF14) | NP_787125.1:n.208+89187_208+89188insC | |
| NR_036486.1:n.410-18244_410-18243insC (FGF14-IT1) | ||
| NM_001321935.1:c.-60+5352_-60+5353insC (FGF14) | NP_001308864.1:n.-60+5352_-60+5353insC | |
| NM_001321936.1:c.-324+5352_-324+5353insC (FGF14) | NP_001308865.1:n.-324+5352_-324+5353insC | |
| NM_001321937.1:c.208+89187_208+89188insC (FGF14) | NP_001308866.1:n.208+89187_208+89188insC | |
| NM_001321938.1:c.-225+89187_-225+89188insC (FGF14) | NP_001308867.1:n.-225+89187_-225+89188insC | |
| NM_001321939.1:c.208+89187_208+89188insC (FGF14) | NP_001308868.1:n.208+89187_208+89188insC | |
| NM_001321940.1:c.-225+89187_-225+89188insC (FGF14) | NP_001308869.1:n.-225+89187_-225+89188insC | |
| NM_001321941.1:c.-60-18244_-60-18243insC (FGF14) | NP_001308870.1:n.-60-18244_-60-18243insC | |
| NM_001321942.1:c.-60+81474_-60+81475insC (FGF14) | NP_001308871.1:n.-60+81474_-60+81475insC | |
| NM_001321943.1:c.-171+89187_-171+89188insC (FGF14) | NP_001308872.1:n.-171+89187_-171+89188insC | |
| NM_001321944.1:c.-324+89187_-324+89188insC (FGF14) | NP_001308873.1:n.-324+89187_-324+89188insC | |
| NM_001321945.1:c.91+89187_91+89188insC (FGF14) | NP_001308874.1:n.91+89187_91+89188insC | |
| NM_001321946.1:c.-60+54161_-60+54162insC (FGF14) | NP_001308875.1:n.-60+54161_-60+54162insC | |
| NM_001321947.1:c.52+89187_52+89188insC (FGF14) | NP_001308876.1:n.52+89187_52+89188insC | |
| NM_001321948.1:c.91+89187_91+89188insC (FGF14) | NP_001308877.1:n.91+89187_91+89188insC | |
| NM_001321949.1:c.-60+54161_-60+54162insC (FGF14) | NP_001308878.1:n.-60+54161_-60+54162insC | |
| XR_001750081.2:n.6248-460_6248-459insG | ||
| NM_001321938.2:c.-225+89187_-225+89188insC (FGF14) | NP_001308867.1:n.-225+89187_-225+89188insC | |
| NM_001321945.2:c.91+89187_91+89188insC (FGF14) | NP_001308874.1:n.91+89187_91+89188insC | |
| NM_001321946.2:c.-60+54161_-60+54162insC (FGF14) | NP_001308875.1:n.-60+54161_-60+54162insC | |
| NM_001321947.2:c.52+89187_52+89188insC (FGF14) | NP_001308876.1:n.52+89187_52+89188insC | |
| NM_001321948.2:c.91+89187_91+89188insC (FGF14) | NP_001308877.1:n.91+89187_91+89188insC | |
| NM_001321937.2:c.208+89187_208+89188insC (FGF14) | NP_001308866.1:n.208+89187_208+89188insC | |
| NM_001321939.2:c.208+89187_208+89188insC (FGF14) | NP_001308868.1:n.208+89187_208+89188insC | |
| NM_001321941.2:c.-60-18244_-60-18243insC (FGF14) | NP_001308870.1:n.-60-18244_-60-18243insC | |
| NM_001379342.1:c.91+89187_91+89188insC (FGF14) | NP_001366271.1:n.91+89187_91+89188insC | |
| NM_175929.3:c.208+89187_208+89188insC (FGF14) | NP_787125.1:n.208+89187_208+89188insC |