Linked Data
gnomAD v2:
11-68682633-C-CTTTTTTTTTTTTTTTTTTTTTTTTTTTT
gnomAD v3:
11-68915165-C-CTTTTTTTTTTTTTTTTTTTTTTTTTTTT
gnomAD v4:
11-68915165-C-CTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68915165_68915166insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915165_68915166insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | GRCh38 |
| NC_000011.9:g.68682633_68682634insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682633_68682634insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | GRCh37 |
| NC_000011.8:g.68439209_68439210insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | NCBI36 |
| NG_007976.1:g.16315_16316insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250:g.16315_16316insTTTTTTTTTTTTTTTTTTTTTTTTTTTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select | ENSP00000255078.4:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTT... | |
| ENST00000539224.2:c.1041+142_1041+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ||
| ENST00000674955.1:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ENSP00000502463.1:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTT... | |
| ENST00000675118.1:c.259+142_259+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ||
| ENST00000675119.1:c.201+142_201+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ENSP00000501861.1:n.201+142_201+143insTTTTTTTTTTTTTTTTTTTTTTT... | |
| ENST00000675305.1:c.201+142_201+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ENSP00000502365.1:n.201+142_201+143insTTTTTTTTTTTTTTTTTTTTTTT... | |
| ENST00000675464.1:c.195+148_195+149insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ENSP00000502650.1:n.195+148_195+149insTTTTTTTTTTTTTTTTTTTTTTT... | |
| ENST00000675615.1:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ENSP00000502413.1:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTT... | |
| ENST00000675683.1:c.299+142_299+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ||
| ENST00000676173.1:n.956+142_956+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ||
| ENST00000676228.1:c.*235+142_*235+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ENSP00000502375.1:n.*235+142_*235+143insTTTTTTTTTTTTTTTTTTTTT... | |
| ENST00000255078.7:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ENSP00000255078.3:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTT... | |
| NM_002180.2:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | NP_002171.2:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | |
| XM_005273974.2:c.-100+142_-100+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | XP_005274031.1:n.-100+142_-100+143insTTTTTTTTTTTTTTTTTTTTTTTT... | |
| XM_005273976.1:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | XP_005274033.1:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTT... | |
| XR_247198.1:n.1014+142_1014+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ||
| XR_949903.1:n.1014+142_1014+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ||
| XM_005273976.2:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | XP_005274033.1:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTT... | |
| XM_017017669.2:c.-100+142_-100+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | XP_016873158.1:n.-100+142_-100+143insTTTTTTTTTTTTTTTTTTTTTTTT... | |
| XM_017017670.2:c.-100+142_-100+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | XP_016873159.1:n.-100+142_-100+143insTTTTTTTTTTTTTTTTTTTTTTTT... | |
| XM_017017671.2:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | XP_016873160.1:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTT... | |
| XR_949903.3:n.1010+142_1010+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT | ||
| NM_002180.3:c.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select | NP_002171.2:n.912+142_912+143insTTTTTTTTTTTTTTTTTTTTTTTTTTTT |