HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152304831_152304835delinsGTGTC , CM000663.2:g.152304831_152304835delinsGTGTC | GRCh38 |
NC_000001.10:g.152277307_152277311delinsGTGTC , CM000663.1:g.152277307_152277311delinsGTGTC | GRCh37 |
NC_000001.9:g.150543931_150543935delinsGTGTC | NCBI36 |
NG_016190.1:g.25369_25373delinsGACAC , LRG_1028:g.25369_25373delinsGACAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.10051_10055delinsGACAC MANE Select | ENSP00000357789.1:p.Asp3351= | |
ENST00000368799.1:c.10051_10055delinsGACAC | ENSP00000357789.1:p.Asp3351= | |
NM_002016.1:c.10051_10055delinsGACAC , LRG_1028t1:c.10051_10055delinsGACAC | NP_002007.1:p.Asp3351= | |
XM_011509329.1:c.9108+943_9108+947delinsGACAC | XP_011507631.1:n.9108+943_9108+947delinsGACAC | |
NM_002016.2:c.10051_10055delinsGACAC MANE Select | NP_002007.1:p.Asp3351= |