HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151100878_151100880dup , CM000667.2:g.151100878_151100880dup | GRCh38 |
NC_000005.9:g.150480439_150480441dup , CM000667.1:g.150480439_150480441dup | GRCh37 |
NC_000005.8:g.150460632_150460634dup | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000354546.10:c.*569_*571dup MANE Select | ENSP00000346550.5:n.*569_*571dup | |
ENST00000522664.5:c.284_286dup | ||
NM_001155.4:c.*569_*571dup | NP_001146.2:n.*569_*571dup | |
NM_001193544.1:c.*569_*571dup | NP_001180473.1:n.*569_*571dup | |
NM_001363114.1:c.*569_*571dup | NP_001350043.1:n.*569_*571dup | |
NM_001155.5:c.*569_*571dup MANE Select | NP_001146.2:n.*569_*571dup | |
NM_001193544.2:c.*569_*571dup | NP_001180473.1:n.*569_*571dup | |
NM_001363114.2:c.*569_*571dup | NP_001350043.1:n.*569_*571dup |