HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667248del , CM000683.2:g.31667248del | GRCh38 |
NC_000021.8:g.33039561del , CM000683.1:g.33039561del | GRCh37 |
NC_000021.7:g.31961432del | NCBI36 |
NG_008689.1:g.12627del , LRG_652:g.12627del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270142.11:c.240-10del MANE Select | ENSP00000270142.7:n.240-10del | |
ENST00000270142.10:c.240-10del | ENSP00000270142.6:n.240-10del | |
ENST00000389995.4:c.183-10del | ENSP00000374645.4:n.183-10del | |
ENST00000470944.1:n.1168-10del | ||
ENST00000476106.5:n.503-10del | ||
NM_000454.4:c.240-10del , LRG_652t1:c.240-10del | NP_000445.1:n.240-10del | |
NM_000454.5:c.240-10del MANE Select | NP_000445.1:n.240-10del |