Linked Data
dbSNP Id:
rs1363057862
gnomAD v2:
11-94199647-T-TTTGTAAAACA
MyVariant Identifiers:
chr11:g.94199647_94199648insTTGTAAAACA (hg19)
chr11:g.94466481_94466482insTTGTAAAACA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.94466481_94466482insTTGTAAAACA , CM000673.2:g.94466481_94466482insTTGTAAAACA | GRCh38 |
| NC_000011.9:g.94199647_94199648insTTGTAAAACA , CM000673.1:g.94199647_94199648insTTGTAAAACA | GRCh37 |
| NC_000011.8:g.93839295_93839296insTTGTAAAACA | NCBI36 |
| NG_007261.1:g.32393_32394insTGTTTTACAA , LRG_85:g.32393_32394insTGTTTTACAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323929.8:c.1098+1331_1098+1332insTGTTTTACAA MANE Select | ENSP00000325863.4:n.1098+1331_1098+1332insTGTTTTACAA | |
| ENST00000323929.7:c.1098+1331_1098+1332insTGTTTTACAA | ENSP00000325863.3:n.1098+1331_1098+1332insTGTTTTACAA | |
| ENST00000323977.7:c.1098+1331_1098+1332insTGTTTTACAA | ENSP00000326094.3:n.1098+1331_1098+1332insTGTTTTACAA | |
| ENST00000393241.8:c.1098+1331_1098+1332insTGTTTTACAA | ENSP00000376933.4:n.1098+1331_1098+1332insTGTTTTACAA | |
| ENST00000407439.7:c.1107+1331_1107+1332insTGTTTTACAA | ENSP00000385614.3:n.1107+1331_1107+1332insTGTTTTACAA | |
| NM_005590.3:c.1098+1331_1098+1332insTGTTTTACAA | NP_005581.2:n.1098+1331_1098+1332insTGTTTTACAA | |
| NM_005591.3:c.1098+1331_1098+1332insTGTTTTACAA , LRG_85t1:c.1098+1331_1098+1332insTGTTTTACAA | NP_005582.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| XM_005274008.2:c.630+1331_630+1332insTGTTTTACAA | XP_005274065.1:n.630+1331_630+1332insTGTTTTACAA | |
| XM_006718842.2:c.1098+1331_1098+1332insTGTTTTACAA | XP_006718905.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| XM_011542837.1:c.1098+1331_1098+1332insTGTTTTACAA | XP_011541139.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| XR_947828.1:n.1394+1331_1394+1332insTGTTTTACAA | ||
| NM_001330347.1:c.1098+1331_1098+1332insTGTTTTACAA | NP_001317276.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| XM_005274008.3:c.630+1331_630+1332insTGTTTTACAA | XP_005274065.1:n.630+1331_630+1332insTGTTTTACAA | |
| XM_006718842.3:c.1098+1331_1098+1332insTGTTTTACAA | XP_006718905.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| XM_011542837.2:c.1098+1331_1098+1332insTGTTTTACAA | XP_011541139.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| XM_017017772.1:c.1098+1331_1098+1332insTGTTTTACAA | XP_016873261.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| XR_947828.2:n.1394+1331_1394+1332insTGTTTTACAA | ||
| NM_001330347.2:c.1098+1331_1098+1332insTGTTTTACAA | NP_001317276.1:n.1098+1331_1098+1332insTGTTTTACAA | |
| NM_005590.4:c.1098+1331_1098+1332insTGTTTTACAA | NP_005581.2:n.1098+1331_1098+1332insTGTTTTACAA | |
| NM_005591.4:c.1098+1331_1098+1332insTGTTTTACAA MANE Select | NP_005582.1:n.1098+1331_1098+1332insTGTTTTACAA |