HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14871599_14871601dup , CM000667.2:g.14871599_14871601dup | GRCh38 |
NC_000005.9:g.14871708_14871710dup , CM000667.1:g.14871708_14871710dup | GRCh37 |
NC_000005.8:g.14924708_14924710dup | NCBI36 |
NG_008273.1:g.5184_5186dup | |
NG_008273.2:g.5191_5193dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284268.8:c.-148_-146dup MANE Select | ENSP00000284268.6:n.-148_-146dup | |
ENST00000284268.6:c.-148_-146dup | ENSP00000284268.6:n.-148_-146dup | |
ENST00000505140.1:c.-148_-146dup | ENSP00000426332.1:n.-148_-146dup | |
NM_054027.4:c.-148_-146dup | NP_473368.1:n.-148_-146dup | |
XM_011514067.1:c.-148_-146dup | XP_011512369.1:n.-148_-146dup | |
NM_054027.5:c.-148_-146dup | NP_473368.1:n.-148_-146dup | |
NM_054027.6:c.-148_-146dup MANE Select | NP_473368.1:n.-148_-146dup |