Linked Data
dbSNP Id:
rs368367806
MyVariant Identifiers:
chr14:g.65543316_65543317insGGG (hg19)
chr14:g.65076598_65076599insGGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65076599_65076600insGGG , CM000676.2:g.65076599_65076600insGGG | GRCh38 |
| NC_000014.8:g.65543317_65543318insGGG , CM000676.1:g.65543317_65543318insGGG | GRCh37 |
| NC_000014.7:g.64613070_64613071insGGG | NCBI36 |
| NG_029830.1:g.30911_30912insCCC , LRG_530:g.30911_30912insCCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000556892.6:c.141_142insCCC | ENSP00000452206.2:p.Asn47_Ser48insPro | |
| ENST00000556979.6:c.*813_*814insCCC | ENSP00000452378.1:n.*813_*814insCCC | |
| ENST00000358664.9:c.360_361insCCC MANE Select | ENSP00000351490.4:p.Asn120_Ser121insPro | |
| ENST00000651648.1:c.145-6230_145-6229insCCC | ENSP00000498863.1:n.145-6230_145-6229insCCC | |
| ENST00000284165.10:c.*1204_*1205insCCC | ENSP00000284165.6:n.*1204_*1205insCCC | |
| ENST00000341653.6:c.171+17109_171+17110insCCC | ENSP00000342482.2:n.171+17109_171+17110insCCC | |
| ENST00000358402.8:c.333_334insCCC | ENSP00000351175.4:p.Asn111_Ser112insPro | |
| ENST00000358664.8:c.360_361insCCC | ENSP00000351490.4:p.Asn120_Ser121insPro | |
| ENST00000394606.6:c.*133_*134insCCC | ENSP00000378104.2:n.*133_*134insCCC | |
| ENST00000553928.5:c.*149_*150insCCC | ENSP00000451907.1:n.*149_*150insCCC | |
| ENST00000555419.5:c.252_253insCCC | ENSP00000452405.1:p.Asn84_Ser85insPro | |
| ENST00000555932.5:c.101_102insCCC | ENSP00000450763.1:p.Thr34_Ala35insPro | |
| ENST00000557277.5:c.171_172insCCC | ENSP00000450955.1:p.Asn57_Ser58insPro | |
| ENST00000618858.4:c.*149_*150insCCC | ENSP00000480127.1:n.*149_*150insCCC | |
| NM_001271069.1:c.144+17109_144+17110insCCC | NP_001257998.1:n.144+17109_144+17110insCCC | |
| NM_002382.4:c.360_361insCCC | NP_002373.3:p.Asn120_Ser121insPro | |
| NM_145112.2:c.333_334insCCC | NP_660087.1:p.Asn111_Ser112insPro | |
| NM_145113.2:c.*149_*150insCCC | NP_660088.1:n.*149_*150insCCC | |
| NM_197957.3:c.171+17109_171+17110insCCC | NP_932061.1:n.171+17109_171+17110insCCC | |
| NR_073137.1:n.484_485insCCC | ||
| XR_429315.2:n.647_648insCCC | ||
| XR_943450.1:n.728_729insCCC | ||
| XR_943451.1:n.744_745insCCC | ||
| XR_943452.1:n.690_691insCCC | ||
| NM_001320415.1:c.171_172insCCC | NP_001307344.1:p.Asn57_Ser58insPro | |
| XM_017021312.2:c.171_172insCCC | XP_016876801.1:p.Asn57_Ser58insPro | |
| XM_017021313.1:c.171_172insCCC | XP_016876802.1:p.Asn57_Ser58insPro | |
| XR_001750326.2:n.705_706insCCC | ||
| XR_001750327.2:n.624_625insCCC | ||
| XR_002957553.1:n.1138_1139insCCC | ||
| XR_943450.3:n.728_729insCCC | ||
| XR_943451.3:n.744_745insCCC | ||
| XR_943452.3:n.689_690insCCC | ||
| NM_001320415.2:c.171_172insCCC | NP_001307344.1:p.Asn57_Ser58insPro | |
| NM_002382.5:c.360_361insCCC MANE Select | NP_002373.3:p.Asn120_Ser121insPro | |
| NM_145112.3:c.333_334insCCC | NP_660087.1:p.Asn111_Ser112insPro | |
| NM_145113.3:c.*149_*150insCCC | NP_660088.1:n.*149_*150insCCC | |
| NM_001271069.2:c.144+17109_144+17110insCCC | NP_001257998.1:n.144+17109_144+17110insCCC | |
| NM_197957.4:c.171+17109_171+17110insCCC | NP_932061.1:n.171+17109_171+17110insCCC |