HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659723del , CM000683.2:g.31659723del | GRCh38 |
NC_000021.8:g.33032036del , CM000683.1:g.33032036del | GRCh37 |
NC_000021.7:g.31953907del | NCBI36 |
NG_008689.1:g.5102del , LRG_652:g.5102del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.-47del MANE Select | ENSP00000270142.7:n.-47del | |
ENST00000270142.10:c.-47del | ENSP00000270142.6:n.-47del | |
ENST00000389995.4:c.-47del | ENSP00000374645.4:n.-47del | |
ENST00000470944.1:n.15del | ||
ENST00000476106.5:n.31del | ||
NM_000454.4:c.-47del , LRG_652t1:c.-47del | NP_000445.1:n.-47del | |
NM_000454.5:c.-47del MANE Select | NP_000445.1:n.-47del |