Linked Data
dbSNP Id:
rs1553157345
MyVariant Identifiers:
chr1:g.65298776_65298777insTTGTTTT (hg19)
chr1:g.64833093_64833094insTTGTTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.64833095_64833096insGTTTTTT , CM000663.2:g.64833095_64833096insGTTTTTT | GRCh38 |
| NC_000001.10:g.65298778_65298779insGTTTTTT , CM000663.1:g.65298778_65298779insGTTTTTT | GRCh37 |
| NC_000001.9:g.65071366_65071367insGTTTTTT | NCBI36 |
| NG_023402.1:g.138411_138412insAAAACAA | |
| NG_023402.2:g.239653_239654insAAAACAA |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000294428.8:c.*2110_*2111insGTTTTTT MANE Select | ENSP00000294428.3:n.*2110_*2111insGTTTTTT... | |
| ENST00000294428.7:c.*2110_*2111insGTTTTTT | ENSP00000294428.3:n.*2110_*2111insGTTTTTT... | |
| ENST00000371072.8:c.*2110_*2111insGTTTTTT | ENSP00000360112.4:n.*2110_*2111insGTTTTTT... | |
| NM_018211.3:c.*2110_*2111insGTTTTTT | NP_060681.2:n.*2110_*2111insGTTTTTT | |
| XM_006710738.2:c.*2110_*2111insGTTTTTT | XP_006710801.2:n.*2110_*2111insGTTTTTT | |
| NM_001366165.1:c.*2110_*2111insGTTTTTT | NP_001353094.1:n.*2110_*2111insGTTTTTT | |
| XR_946693.3:n.4529_4530insGTTTTTT | ||
| NM_018211.4:c.*2110_*2111insGTTTTTT | NP_060681.2:n.*2110_*2111insGTTTTTT | |
| NM_001366165.2:c.*2110_*2111insGTTTTTT MANE Select | NP_001353094.1:n.*2110_*2111insGTTTTTT |