HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99949522dup , CM000666.2:g.99949522dup | GRCh38 |
NC_000004.11:g.100870679dup , CM000666.1:g.100870679dup | GRCh37 |
NC_000004.10:g.101089702dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296417.6:c.82-136dup MANE Select | ENSP00000296417.5:n.82-136dup | |
ENST00000651623.1:c.82-136dup | ENSP00000498935.1:n.82-136dup | |
ENST00000296417.5:c.82-136dup | ENSP00000296417.5:n.82-136dup | |
ENST00000511203.1:n.778dup | ||
ENST00000511319.5:n.607-136dup | ||
ENST00000511348.1:n.407dup | ||
ENST00000527366.1:n.165+141dup | ||
ENST00000529158.5:n.131-136dup | ||
NM_002106.3:c.82-136dup | NP_002097.1:n.82-136dup | |
NM_002106.4:c.82-136dup MANE Select | NP_002097.1:n.82-136dup |