Linked Data
gnomAD v2:
17-61565950-C-CTGTCG
MyVariant Identifiers:
chr17:g.61565950_61565951insTGTCG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63488589_63488590insTGTCG , CM000679.2:g.63488589_63488590insTGTCG | GRCh38 |
| NC_000017.10:g.61565950_61565951insTGTCG , CM000679.1:g.61565950_61565951insTGTCG | GRCh37 |
| NC_000017.9:g.58919682_58919683insTGTCG | NCBI36 |
| NG_011648.1:g.16517_16518insTGTCG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000290866.10:c.2306-59_2306-58insTGTCG MANE Select | ENSP00000290866.4:n.2306-59_2306-58insTGT... | |
| ENST00000290863.10:c.584-59_584-58insTGTCG | ENSP00000290863.6:n.584-59_584-58insTGTCG... | |
| ENST00000290866.9:c.2306-59_2306-58insTGTCG | ENSP00000290866.4:n.2306-59_2306-58insTGT... | |
| ENST00000413513.7:c.584-59_584-58insTGTCG | ENSP00000392247.3:n.584-59_584-58insTGTCG... | |
| ENST00000428043.5:c.2306-59_2306-58insTGTCG | ENSP00000397593.2:n.2306-59_2306-58insTGT... | |
| ENST00000577647.2:c.584-59_584-58insTGTCG | ENSP00000464149.1:n.584-59_584-58insTGTCG... | |
| ENST00000578839.5:c.*376-59_*376-58insTGTCG | ENSP00000462110.2:n.*376-59_*376-58insTGT... | |
| ENST00000579204.1:c.506_507insTGTCG | ENSP00000464629.1:n.506_507insTGTCG | |
| ENST00000579314.5:c.603_604insTGTCG | ENSP00000462599.1:p.Pro202CysfsTer8 | |
| ENST00000582005.5:c.*226-59_*226-58insTGTCG | ENSP00000462002.1:n.*226-59_*226-58insTGT... | |
| ENST00000582761.1:c.74-59_74-58insTGTCG | ENSP00000462909.1:n.74-59_74-58insTGTCG | |
| ENST00000584865.5:n.252-59_252-58insTGTCG | ||
| NM_000789.3:c.2306-59_2306-58insTGTCG | NP_000780.1:n.2306-59_2306-58insTGTCG | |
| NM_001178057.1:c.584-59_584-58insTGTCG | NP_001171528.1:n.584-59_584-58insTGTCG | |
| NM_152830.2:c.584-59_584-58insTGTCG | NP_690043.1:n.584-59_584-58insTGTCG | |
| XM_005257110.1:c.1757-59_1757-58insTGTCG | XP_005257167.1:n.1757-59_1757-58insTGTCG | |
| XM_006721737.2:c.644-59_644-58insTGTCG | XP_006721800.2:n.644-59_644-58insTGTCG | |
| XM_006721737.3:c.644-59_644-58insTGTCG | XP_006721800.2:n.644-59_644-58insTGTCG | |
| NM_000789.4:c.2306-59_2306-58insTGTCG MANE Select | NP_000780.1:n.2306-59_2306-58insTGTCG | |
| NM_001178057.2:c.584-59_584-58insTGTCG | NP_001171528.1:n.584-59_584-58insTGTCG | |
| NM_152830.3:c.584-59_584-58insTGTCG | NP_690043.1:n.584-59_584-58insTGTCG | |
| NM_001382700.1:c.1739-59_1739-58insTGTCG | NP_001369629.1:n.1739-59_1739-58insTGTCG | |
| NM_001382701.1:c.1454-59_1454-58insTGTCG | NP_001369630.1:n.1454-59_1454-58insTGTCG | |
| NM_001382702.1:c.236-59_236-58insTGTCG | NP_001369631.1:n.236-59_236-58insTGTCG | |
| NR_168483.1:n.625_626insTGTCG |