Linked Data
gnomAD v2:
11-70319213-GTTGCAGTATC-G
MyVariant Identifiers:
chr11:g.70319214_70319225delinsGA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.70473109_70473118del , CM000673.2:g.70473109_70473118del | GRCh38 |
| NC_000011.9:g.70319214_70319223del , CM000673.1:g.70319214_70319223del | GRCh37 |
| NC_000011.8:g.69996862_69996871del | NCBI36 |
| NG_042866.1:g.656679_656688del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338508.9:c.3534_3543del | ENSP00000345193.7:p.Ile1179SerfsTer28 | |
| ENST00000412252.6:c.1079_1088del | ENSP00000414876.2:n.1079_1088del | |
| ENST00000601538.6:c.5301_5310del MANE Select | ENSP00000469689.2:p.Ile1768SerfsTer28 | |
| ENST00000654939.1:c.2810_2819del | ||
| ENST00000656230.1:c.4164_4173del | ENSP00000499561.1:p.Ile1389SerfsTer28 | |
| ENST00000659264.1:c.3591_3600del | ENSP00000499270.1:p.Ile1198SerfsTer28 | |
| ENST00000338508.8:c.3537_3546del | ENSP00000345193.6:p.Ile1180SerfsTer28 | |
| ENST00000357171.7:c.*305_*314del | ENSP00000349694.4:n.*305_*314del | |
| ENST00000409161.5:c.3513_3522del | ENSP00000386491.1:p.Ile1172SerfsTer28 | |
| ENST00000412252.5:c.1077_1086del | ||
| ENST00000423696.6:c.4164_4173del | ENSP00000394536.2:p.Ile1389SerfsTer28 | |
| ENST00000424924.5:c.3138_3147del | ENSP00000402944.1:p.Ile1047SerfsTer28 | |
| ENST00000449833.6:c.3537_3546del | ENSP00000399423.3:p.Ile1180SerfsTer28 | |
| ENST00000601538.5:c.5301_5310del | ENSP00000469689.2:p.Ile1768SerfsTer28 | |
| ENST00000606715.3:n.2053_2062del | ||
| NM_012309.4:c.5301_5310del | NP_036441.2:p.Ile1768SerfsTer28 | |
| NM_133266.4:c.3537_3546del | NP_573573.2:p.Ile1180SerfsTer28 | |
| NR_110766.1:n.1155_1164del | ||
| XM_005277930.2:c.5301_5310del | XP_005277987.1:p.Ile1768SerfsTer28 | |
| XM_005277932.2:c.4164_4173del | XP_005277989.1:p.Ile1389SerfsTer28 | |
| XM_006718478.2:c.5271_5280del | XP_006718541.1:p.Ile1758SerfsTer28 | |
| XM_011544854.1:c.5313_5322del | XP_011543156.1:p.Ile1772SerfsTer28 | |
| XM_011544855.1:c.5292_5301del | XP_011543157.1:p.Ile1765SerfsTer28 | |
| XM_011544856.1:c.5286_5295del | XP_011543158.1:p.Ile1763SerfsTer28 | |
| XM_011544857.1:c.5265_5274del | XP_011543159.1:p.Ile1756SerfsTer28 | |
| XM_011544859.1:c.4176_4185del | XP_011543161.1:p.Ile1393SerfsTer28 | |
| XM_005277932.3:c.4164_4173del | XP_005277989.1:p.Ile1389SerfsTer28 | |
| XM_017017387.1:c.5301_5310del | XP_016872876.1:p.Ile1768SerfsTer28 | |
| XM_017017388.1:c.5301_5310del | XP_016872877.1:p.Ile1768SerfsTer28 | |
| XM_017017389.1:c.5274_5283del | XP_016872878.1:p.Ile1759SerfsTer28 | |
| XM_017017390.1:c.3591_3600del | XP_016872879.1:p.Ile1198SerfsTer28 | |
| NM_133266.5:c.3537_3546del | NP_573573.2:p.Ile1180SerfsTer28 | |
| NR_110766.2:n.1156_1165del | ||
| NM_001379226.1:c.4164_4173del | NP_001366155.1:p.Ile1389SerfsTer28 | |
| NM_012309.5:c.5301_5310del MANE Select | NP_036441.2:p.Ile1768SerfsTer28 |