HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8732061_8732066del , CM000685.2:g.8732061_8732066del | GRCh38 |
NC_000023.10:g.8700102_8700107del , CM000685.1:g.8700102_8700107del | GRCh37 |
NC_000023.9:g.8660102_8660107del | NCBI36 |
NG_007088.1:g.5135_5140del | |
NG_007088.2:g.5135_5140del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.-16_-11del MANE Select | ENSP00000262648.3:n.-16_-11del | |
ENST00000262648.7:c.-16_-11del | ENSP00000262648.3:n.-16_-11del | |
ENST00000619786.1:c.-16_-11del | ENSP00000478734.1:n.-16_-11del | |
NM_000216.2:c.-16_-11del | NP_000207.2:n.-16_-11del | |
XM_005274501.3:c.-16_-11del | XP_005274558.1:n.-16_-11del | |
NM_000216.3:c.-16_-11del | NP_000207.2:n.-16_-11del | |
XM_005274501.4:c.-16_-11del | XP_005274558.1:n.-16_-11del | |
NM_000216.4:c.-16_-11del MANE Select | NP_000207.2:n.-16_-11del |