HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114135_140114137dup , CM000667.2:g.140114135_140114137dup | GRCh38 |
NC_000005.9:g.139493720_139493722dup , CM000667.1:g.139493720_139493722dup | GRCh37 |
NC_000005.8:g.139473904_139473906dup | NCBI36 |
NG_041813.1:g.5013_5015dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.-47_-45dup MANE Select | ENSP00000332706.3:n.-47_-45dup | |
ENST00000505703.2:c.-47_-45dup | ENSP00000498560.1:n.-47_-45dup | |
ENST00000651386.1:c.-47_-45dup | ENSP00000499133.1:n.-47_-45dup | |
ENST00000331327.4:c.-47_-45dup | ENSP00000332706.3:n.-47_-45dup | |
ENST00000502351.1:n.377_379dup | ||
ENST00000505703.1:n.419_421dup | ||
NM_005859.4:c.-47_-45dup | NP_005850.1:n.-47_-45dup | |
NM_005859.5:c.-47_-45dup MANE Select | NP_005850.1:n.-47_-45dup |