Linked Data
dbSNP Id:
rs1221394315
gnomAD v2:
15-43893787-G-GTAA
gnomAD v3:
15-43601589-G-GTAA
gnomAD v4:
15-43601589-G-GTAA
MyVariant Identifiers:
chr15:g.43893787_43893788insTAA (hg19)
chr15:g.43601589_43601590insTAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.43601590_43601591insAAT , CM000677.2:g.43601590_43601591insAAT | GRCh38 |
| NC_000015.9:g.43893788_43893789insAAT , CM000677.1:g.43893788_43893789insAAT | GRCh37 |
| NC_000015.8:g.41681080_41681081insAAT | NCBI36 |
| NG_011636.1:g.22211_22212insTTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450892.7:c.4546-39_4546-38insTTA (STRC) MANE Select | ENSP00000401513.2:n.4546-39_4546-38insTTA | |
| ENST00000411560.1:n.142+2057_142+2058insAAT (CKMT1B) | ||
| ENST00000428650.5:c.*1579-39_*1579-38insTTA (STRC) | ENSP00000415991.1:n.*1579-39_*1579-38insTTA | |
| ENST00000440125.5:c.*2338-39_*2338-38insTTA (STRC) | ENSP00000394866.1:n.*2338-39_*2338-38insTTA | |
| ENST00000448437.6:n.1666-39_1666-38insTTA (STRC) | ||
| ENST00000450892.6:c.4546-39_4546-38insTTA (STRC) | ENSP00000401513.2:n.4546-39_4546-38insTTA | |
| ENST00000460952.1:n.86_87insTTA (STRC) | ||
| ENST00000471703.5:n.2500-39_2500-38insTTA (STRC) | ||
| ENST00000485556.5:n.3401-39_3401-38insTTA (STRC) | ||
| ENST00000493750.1:n.342-39_342-38insTTA (STRC) | ||
| ENST00000541030.5:c.2227-39_2227-38insTTA (STRC) | ENSP00000440413.1:n.2227-39_2227-38insTTA | |
| NM_153700.2:c.4546-39_4546-38insTTA (STRC) MANE Select | NP_714544.1:n.4546-39_4546-38insTTA | |
| XM_011521277.1:c.5035-39_5035-38insTTA (STRC) | XP_011519579.1:n.5035-39_5035-38insTTA | |
| XM_011521278.1:c.4651-39_4651-38insTTA (STRC) | XP_011519580.1:n.4651-39_4651-38insTTA | |
| XM_011521279.1:c.4651-39_4651-38insTTA (STRC) | XP_011519581.1:n.4651-39_4651-38insTTA |