HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29073165_29073173del , CM000664.2:g.29073165_29073173del | GRCh38 |
NC_000002.11:g.29296031_29296039del , CM000664.1:g.29296031_29296039del | GRCh37 |
NC_000002.10:g.29149535_29149543del | NCBI36 |
NG_021427.1:g.6094_6102del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.1094_1102del MANE Select | ENSP00000332809.4:p.Leu365_Lys367del | |
ENST00000331664.5:c.1094_1102del | ENSP00000332809.4:p.Leu365_Lys367del | |
NM_001029883.2:c.1094_1102del | NP_001025054.1:p.Leu365_Lys367del | |
XM_011532826.1:c.1094_1102del | XP_011531128.1:p.Leu365_Lys367del | |
XR_939901.1:n.185+3998_185+4006del | ||
XR_939902.1:n.173+4010_173+4018del | ||
NM_001029883.3:c.1094_1102del MANE Select | NP_001025054.1:p.Leu365_Lys367del |