HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151100935_151100938dup , CM000667.2:g.151100935_151100938dup | GRCh38 |
NC_000005.9:g.150480496_150480499dup , CM000667.1:g.150480496_150480499dup | GRCh37 |
NC_000005.8:g.150460689_150460692dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354546.10:c.*510_*513dup MANE Select | ENSP00000346550.5:n.*510_*513dup | |
ENST00000522664.5:c.225_228dup | ||
NM_001155.4:c.*510_*513dup | NP_001146.2:n.*510_*513dup | |
NM_001193544.1:c.*510_*513dup | NP_001180473.1:n.*510_*513dup | |
NM_001363114.1:c.*510_*513dup | NP_001350043.1:n.*510_*513dup | |
NM_001155.5:c.*510_*513dup MANE Select | NP_001146.2:n.*510_*513dup | |
NM_001193544.2:c.*510_*513dup | NP_001180473.1:n.*510_*513dup | |
NM_001363114.2:c.*510_*513dup | NP_001350043.1:n.*510_*513dup |