HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147200426del , CM000669.2:g.147200426del | GRCh38 |
NC_000007.13:g.146897518del , CM000669.1:g.146897518del | GRCh37 |
NC_000007.12:g.146528451del | NCBI36 |
NG_007092.2:g.1089066del | |
NG_007092.3:g.1089426del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.1348+67917del MANE Select | ENSP00000354778.3:n.1348+67917del | |
ENST00000636870.1:n.1210+67917del | ||
ENST00000637694.1:n.1251+67917del | ||
ENST00000637825.1:n.831+67917del | ||
ENST00000638117.1:n.1251+67917del | ||
ENST00000361727.7:c.1348+67917del | ENSP00000354778.3:n.1348+67917del | |
NM_014141.5:c.1348+67917del | NP_054860.1:n.1348+67917del | |
XM_017011950.2:c.1348+67917del | XP_016867439.1:n.1348+67917del | |
NM_014141.6:c.1348+67917del MANE Select | NP_054860.1:n.1348+67917del |