MyVariant.info:
GRCh37
chr11:g.119077161del
gnomAD v2:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119206455del , CM000673.2:g.119206455del | GRCh38 |
| NC_000011.9:g.119077165del , CM000673.1:g.119077165del | GRCh37 |
| NC_000011.8:g.118582375del | NCBI36 |
| NG_016808.1:g.5176del , LRG_608:g.5176del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700472.1:c.38del | ENSP00000515005.1:p.Gly13AlafsTer13 | |
| ENST00000264033.6:c.38del MANE Select | ENSP00000264033.3:p.Gly13AlafsTer13 | |
| ENST00000637974.1:c.32del | ENSP00000490763.1:p.Gly11AlafsTer13 | |
| ENST00000264033.5:c.38del | ENSP00000264033.3:p.Gly13AlafsTer13 | |
| ENST00000634586.1:c.38del | ENSP00000489218.1:p.Gly13AlafsTer13 | |
| ENST00000634840.1:c.38del | ENSP00000489324.1:p.Gly13AlafsTer13 | |
| NM_005188.3:c.38del , LRG_608t1:c.38del | NP_005179.2:p.Gly13AlafsTer13 | |
| XM_011543057.1:c.38del | XP_011541359.1:p.Gly13AlafsTer13 | |
| NM_005188.4:c.38del MANE Select | NP_005179.2:p.Gly13AlafsTer13 |