HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154953935_154953952del , CM000685.2:g.154953935_154953952del | GRCh38 |
NC_000023.10:g.154182210_154182227del , CM000685.1:g.154182210_154182227del | GRCh37 |
NC_000023.9:g.153835404_153835421del | NCBI36 |
NG_011403.1:g.73773_73790del | |
NG_011403.2:g.73773_73790del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1844_1861del MANE Select | ENSP00000353393.4:p.Pro615_Val620del | |
ENST00000647125.1:c.*1720_*1737del | ENSP00000496062.1:n.*1720_*1737del | |
ENST00000360256.8:c.1844_1861del | ENSP00000353393.4:p.Pro615_Val620del | |
NM_000132.3:c.1844_1861del | NP_000123.1:p.Pro615_Val620del | |
XM_011531126.1:c.1739_1756del | XP_011529428.1:p.Pro580_Val585del | |
NM_000132.4:c.1844_1861del MANE Select | NP_000123.1:p.Pro615_Val620del |