HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44290898del , CM000683.2:g.44290898del | GRCh38 |
NC_000021.8:g.45710781del , CM000683.1:g.45710781del | GRCh37 |
NC_000021.7:g.44535209del | NCBI36 |
NG_009556.1:g.10019del , LRG_18:g.10019del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.880-197del MANE Select | ENSP00000291582.5:n.880-197del | |
ENST00000291582.5:c.880-197del | ENSP00000291582.5:n.880-197del | |
ENST00000337909.5:n.144del | ||
ENST00000397994.8:n.144del | ||
ENST00000527919.5:n.1613-200del | ||
ENST00000530812.5:n.2630-200del | ||
NM_000383.3:c.880-197del | NP_000374.1:n.880-197del | |
XM_011529551.1:c.880-200del | XP_011527853.1:n.880-200del | |
NM_000383.4:c.880-197del MANE Select | NP_000374.1:n.880-197del |