Linked Data
dbSNP Id:
rs779671276
MyVariant Identifiers:
chr3:g.46901082_46901083insTGTCCCTGG (hg19)
chr3:g.46859592_46859593insTGTCCCTGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46859592_46859593insTGTCCCTGG , CM000665.2:g.46859592_46859593insTGTCCCTGG | GRCh38 |
| NC_000003.11:g.46901082_46901083insTGTCCCTGG , CM000665.1:g.46901082_46901083insTGTCCCTGG | GRCh37 |
| NC_000003.10:g.46876086_46876087insTGTCCCTGG | NCBI36 |
| NG_007555.2:g.27577_27578insCCAGGGACA , LRG_395:g.27577_27578insCCAGGGACA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000431168.2:c.363_364insCCAGGGACA | ENSP00000393455.2:p.Ile121_Ser122insProGlyThr | |
| ENST00000292327.6:c.363_364insCCAGGGACA MANE Select | ENSP00000292327.4:p.Ile121_Ser122insProGlyThr | |
| ENST00000653454.1:c.363_364insCCAGGGACA | ENSP00000499624.1:p.Ile121_Ser122insProGlyThr | |
| ENST00000654597.1:c.363_364insCCAGGGACA | ENSP00000499406.1:p.Ile121_Ser122insProGlyThr | |
| ENST00000655244.1:n.585_586insCCAGGGACA | ||
| ENST00000662933.1:c.363_364insCCAGGGACA | ENSP00000499577.1:p.Ile121_Ser122insProGlyThr | |
| ENST00000664891.1:n.321_322insCCAGGGACA | ||
| ENST00000292327.4:c.363_364insCCAGGGACA | ENSP00000292327.4:p.Ile121_Ser122insProGlyThr | |
| ENST00000395869.5:c.363_364insCCAGGGACA | ENSP00000379210.1:p.Ile121_Ser122insProGlyThr | |
| NM_000258.2:c.363_364insCCAGGGACA , LRG_395t1:c.363_364insCCAGGGACA | NP_000249.1:p.Ile121_Ser122insProGlyThr | |
| NM_000258.3:c.363_364insCCAGGGACA MANE Select | NP_000249.1:p.Ile121_Ser122insProGlyThr |