Linked Data
dbSNP Id:
rs1403335071
MyVariant Identifiers:
chr3:g.128780343_128780344insTCCCAATC (hg19)
chr3:g.129061500_129061501insTCCCAATC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129061500_129061501insTCCCAATC , CM000665.2:g.129061500_129061501insTCCCAATC | GRCh38 |
| NC_000003.11:g.128780343_128780344insTCCCAATC , CM000665.1:g.128780343_128780344insTCCCAATC | GRCh37 |
| NC_000003.10:g.130263033_130263034insTCCCAATC | NCBI36 |
| NG_008715.1:g.5699_5700insTCCCAATC , LRG_477:g.5699_5700insTCCCAATC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307395.5:c.-132_-131insTCCCAATC MANE Select | ENSP00000303942.4:n.-132_-131insTCCCAATC | |
| ENST00000307395.4:c.-132_-131insTCCCAATC | ENSP00000303942.4:n.-132_-131insTCCCAATC | |
| NM_000174.4:c.-132_-131insTCCCAATC , LRG_477t1:c.-132_-131insTCCCAATC | NP_000165.1:n.-132_-131insTCCCAATC | |
| XM_005247374.3:c.-132_-131insTCCCAATC | XP_005247431.1:n.-132_-131insTCCCAATC | |
| XM_011512701.1:c.-132_-131insTCCCAATC | XP_011511003.1:n.-132_-131insTCCCAATC | |
| XM_011512702.1:c.-12-228_-12-227insTCCCAATC | XP_011511004.1:n.-12-228_-12-227insTCCCAATC | |
| NM_000174.5:c.-132_-131insTCCCAATC MANE Select | NP_000165.1:n.-132_-131insTCCCAATC |