UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
gnomAD v4:
2-26475814-G-GGCTCACAGGCCCCACAGGCTCCAGT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26475814_26475815insGCTCACAGGCCCCACAGGCTCCAGT , CM000664.2:g.26475814_26475815insGCTCACAGGCCCCACAGGCTCCAGT | GRCh38 |
| NC_000002.11:g.26698682_26698683insGCTCACAGGCCCCACAGGCTCCAGT , CM000664.1:g.26698682_26698683insGCTCACAGGCCCCACAGGCTCCAGT | GRCh37 |
| NC_000002.10:g.26552186_26552187insGCTCACAGGCCCCACAGGCTCCAGT | NCBI36 |
| NG_009937.1:g.87884_87885insACTGGAGCCTGTGGGGCCTGTGAGC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000272371.7:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC MANE Select | ENSP00000272371.2:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTG... | |
| ENST00000339598.8:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC MANE Plus Clinical | ENSP00000344521.3:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAG... | |
| ENST00000402415.8:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | ENSP00000383906.4:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAG... | |
| ENST00000272371.6:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | ENSP00000272371.2:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTG... | |
| ENST00000338581.10:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | ENSP00000345137.6:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAG... | |
| ENST00000339598.7:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | ENSP00000344521.3:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAG... | |
| ENST00000402415.7:c.921+99_921+100insACTGGAGCCTGTGGGGCCTGTGAGC | ENSP00000383906.3:n.921+99_921+100insACTGGAGCCTGTGGGGCCTGTGAG... | |
| ENST00000403946.7:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | ENSP00000385255.3:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTG... | |
| NM_001287489.1:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_001274418.1:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC... | |
| NM_004802.3:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_004793.2:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | |
| NM_194248.2:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_919224.1:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | |
| NM_194322.2:c.921+99_921+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_919303.1:n.921+99_921+100insACTGGAGCCTGTGGGGCCTGTGAGC | |
| NM_194323.2:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_919304.1:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | |
| XM_005264644.2:c.3036+99_3036+100insACTGGAGCCTGTGGGGCCTGTGAGC | XP_005264701.1:n.3036+99_3036+100insACTGGAGCCTGTGGGGCCTGTGAGC... | |
| XM_011533185.1:c.3036+99_3036+100insACTGGAGCCTGTGGGGCCTGTGAGC | XP_011531487.1:n.3036+99_3036+100insACTGGAGCCTGTGGGGCCTGTGAGC... | |
| XM_017005338.1:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | XP_016860827.1:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC... | |
| NM_001287489.2:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_001274418.1:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC... | |
| NM_004802.4:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_004793.2:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC | |
| NM_194248.3:c.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC MANE Select | NP_919224.1:n.2991+99_2991+100insACTGGAGCCTGTGGGGCCTGTGAGC | |
| NM_194322.3:c.921+99_921+100insACTGGAGCCTGTGGGGCCTGTGAGC | NP_919303.1:n.921+99_921+100insACTGGAGCCTGTGGGGCCTGTGAGC | |
| NM_194323.3:c.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC MANE Plus Clinical | NP_919304.1:n.750+99_750+100insACTGGAGCCTGTGGGGCCTGTGAGC |