HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003825_47003833del , CM000681.2:g.47003825_47003833del | GRCh38 |
NC_000019.9:g.47507082_47507090del , CM000681.1:g.47507082_47507090del | GRCh37 |
NC_000019.8:g.52198922_52198930del | NCBI36 |
NG_047014.1:g.90259_90267del | |
NG_047014.2:g.147829_147837del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7637_7645del | ENSP00000385720.2:n.7637_7645del | |
ENST00000672722.1:c.*3137_*3145del MANE Select | ENSP00000500409.1:n.*3137_*3145del | |
ENST00000404338.7:c.7637_7645del | ENSP00000385720.2:n.7637_7645del | |
ENST00000614079.1:c.7214_7222del | ENSP00000483730.1:n.7214_7222del | |
NM_004491.4:c.7637_7645del | NP_004482.4:n.7637_7645del | |
NM_004491.5:c.*3137_*3145del MANE Select | NP_004482.4:n.*3137_*3145del |