HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14871572_14871588dup , CM000667.2:g.14871572_14871588dup | GRCh38 |
NC_000005.9:g.14871681_14871697dup , CM000667.1:g.14871681_14871697dup | GRCh37 |
NC_000005.8:g.14924681_14924697dup | NCBI36 |
NG_008273.1:g.5192_5208dup | |
NG_008273.2:g.5199_5215dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284268.8:c.-140_-124dup MANE Select | ENSP00000284268.6:n.-140_-124dup | |
ENST00000284268.6:c.-140_-124dup | ENSP00000284268.6:n.-140_-124dup | |
ENST00000505140.1:c.-140_-124dup | ENSP00000426332.1:n.-140_-124dup | |
NM_054027.4:c.-140_-124dup | NP_473368.1:n.-140_-124dup | |
XM_011514067.1:c.-140_-124dup | XP_011512369.1:n.-140_-124dup | |
NM_054027.5:c.-140_-124dup | NP_473368.1:n.-140_-124dup | |
NM_054027.6:c.-140_-124dup MANE Select | NP_473368.1:n.-140_-124dup |