HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152304762_152304858del , CM000663.2:g.152304762_152304858del | GRCh38 |
NC_000001.10:g.152277238_152277334del , CM000663.1:g.152277238_152277334del | GRCh37 |
NC_000001.9:g.150543862_150543958del | NCBI36 |
NG_016190.1:g.25348_25444del , LRG_1028:g.25348_25444del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.10030_10126del MANE Select | ENSP00000357789.1:p.Glu3344GlnfsTer15 | |
ENST00000368799.1:c.10030_10126del | ENSP00000357789.1:p.Glu3344GlnfsTer15 | |
NM_002016.1:c.10030_10126del , LRG_1028t1:c.10030_10126del | NP_002007.1:p.Glu3344GlnfsTer15 | |
XM_011509329.1:c.9108+922_9109-927del | XP_011507631.1:n.9108+922_9109-927del | |
NM_002016.2:c.10030_10126del MANE Select | NP_002007.1:p.Glu3344GlnfsTer15 |