Linked Data
gnomAD v2:
11-68682673-G-GTTTTTTTT
gnomAD v3:
11-68915205-G-GTTTTTTTT
gnomAD v4:
11-68915205-G-GTTTTTTTT
MyVariant Identifiers:
chr11:g.68682673_68682674insTTTTTTTT (hg19)
chr11:g.68915205_68915206insTTTTTTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68915209_68915210insTTTTTTTT , CM000673.2:g.68915209_68915210insTTTTTTTT | GRCh38 |
| NC_000011.9:g.68682677_68682678insTTTTTTTT , CM000673.1:g.68682677_68682678insTTTTTTTT | GRCh37 |
| NC_000011.8:g.68439253_68439254insTTTTTTTT | NCBI36 |
| NG_007976.1:g.16359_16360insTTTTTTTT , LRG_250:g.16359_16360insTTTTTTTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.912+186_912+187insTTTTTTTT MANE Select | ENSP00000255078.4:n.912+186_912+187insTTTTTTTT | |
| ENST00000539224.2:c.1041+186_1041+187insTTTTTTTT | ||
| ENST00000674955.1:c.912+186_912+187insTTTTTTTT | ENSP00000502463.1:n.912+186_912+187insTTTTTTTT | |
| ENST00000675118.1:c.259+186_259+187insTTTTTTTT | ||
| ENST00000675119.1:c.201+186_201+187insTTTTTTTT | ENSP00000501861.1:n.201+186_201+187insTTTTTTTT | |
| ENST00000675305.1:c.201+186_201+187insTTTTTTTT | ENSP00000502365.1:n.201+186_201+187insTTTTTTTT | |
| ENST00000675464.1:c.195+192_195+193insTTTTTTTT | ENSP00000502650.1:n.195+192_195+193insTTTTTTTT | |
| ENST00000675615.1:c.912+186_912+187insTTTTTTTT | ENSP00000502413.1:n.912+186_912+187insTTTTTTTT | |
| ENST00000675683.1:c.299+186_299+187insTTTTTTTT | ||
| ENST00000676173.1:n.956+186_956+187insTTTTTTTT | ||
| ENST00000676228.1:c.*235+186_*235+187insTTTTTTTT | ENSP00000502375.1:n.*235+186_*235+187insTTTTTTTT | |
| ENST00000255078.7:c.912+186_912+187insTTTTTTTT | ENSP00000255078.3:n.912+186_912+187insTTTTTTTT | |
| NM_002180.2:c.912+186_912+187insTTTTTTTT , LRG_250t1:c.912+186_912+187insTTTTTTTT | NP_002171.2:n.912+186_912+187insTTTTTTTT | |
| XM_005273974.2:c.-100+186_-100+187insTTTTTTTT | XP_005274031.1:n.-100+186_-100+187insTTTTTTTT | |
| XM_005273976.1:c.912+186_912+187insTTTTTTTT | XP_005274033.1:n.912+186_912+187insTTTTTTTT | |
| XR_247198.1:n.1014+186_1014+187insTTTTTTTT | ||
| XR_949903.1:n.1014+186_1014+187insTTTTTTTT | ||
| XM_005273976.2:c.912+186_912+187insTTTTTTTT | XP_005274033.1:n.912+186_912+187insTTTTTTTT | |
| XM_017017669.2:c.-100+186_-100+187insTTTTTTTT | XP_016873158.1:n.-100+186_-100+187insTTTTTTTT | |
| XM_017017670.2:c.-100+186_-100+187insTTTTTTTT | XP_016873159.1:n.-100+186_-100+187insTTTTTTTT | |
| XM_017017671.2:c.912+186_912+187insTTTTTTTT | XP_016873160.1:n.912+186_912+187insTTTTTTTT | |
| XR_949903.3:n.1010+186_1010+187insTTTTTTTT | ||
| NM_002180.3:c.912+186_912+187insTTTTTTTT MANE Select | NP_002171.2:n.912+186_912+187insTTTTTTTT |