HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48487464del , CM000677.2:g.48487464del | GRCh38 |
NC_000015.9:g.48779661del , CM000677.1:g.48779661del | GRCh37 |
NC_000015.8:g.46566953del | NCBI36 |
NG_008805.2:g.163327del , LRG_778:g.163327del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.3338-25del | ENSP00000453958.2:n.3338-25del | |
ENST00000674301.2:c.3338-25del | ENSP00000501333.2:n.3338-25del | |
ENST00000684448.1:n.2012-25del | ||
ENST00000316623.10:c.3338-25del MANE Select | ENSP00000325527.5:n.3338-25del | |
ENST00000316623.9:c.3338-25del | ENSP00000325527.5:n.3338-25del | |
ENST00000537463.6:c.637-12812del | ENSP00000440294.2:n.637-12812del | |
NM_000138.4:c.3338-25del , LRG_778t1:c.3338-25del | NP_000129.3:n.3338-25del | |
NM_000138.5:c.3338-25del MANE Select | NP_000129.3:n.3338-25del |