HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154954020del , CM000685.2:g.154954020del | GRCh38 |
NC_000023.10:g.154182295del , CM000685.1:g.154182295del | GRCh37 |
NC_000023.9:g.153835489del | NCBI36 |
NG_011403.1:g.73704del | |
NG_011403.2:g.73704del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1775del MANE Select | ENSP00000353393.4:p.Val592AlafsTer? | |
ENST00000647125.1:c.*1651del | ENSP00000496062.1:n.*1651del | |
ENST00000360256.8:c.1775del | ENSP00000353393.4:p.Val592AlafsTer? | |
NM_000132.3:c.1775del | NP_000123.1:p.Val592AlafsTer? | |
XM_011531126.1:c.1670del | XP_011529428.1:p.Val557AlafsTer? | |
NM_000132.4:c.1775del MANE Select | NP_000123.1:p.Val592AlafsTer? |