HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188868_20188871del , CM000675.2:g.20188868_20188871del | GRCh38 |
NC_000013.10:g.20763007_20763010del , CM000675.1:g.20763007_20763010del | GRCh37 |
NC_000013.9:g.19661007_19661010del | NCBI36 |
NG_008358.1:g.9107_9110del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.*32_*35del | ENSP00000372295.1:n.*32_*35del | |
ENST00000382848.5:c.*32_*35del MANE Select | ENSP00000372299.4:n.*32_*35del | |
ENST00000382844.1:c.*32_*35del | ENSP00000372295.1:n.*32_*35del | |
ENST00000382848.4:c.*32_*35del | ENSP00000372299.4:n.*32_*35del | |
NM_004004.5:c.*32_*35del | NP_003995.2:n.*32_*35del | |
XM_011535049.1:c.*32_*35del | XP_011533351.1:n.*32_*35del | |
XM_011535049.2:c.*32_*35del | XP_011533351.1:n.*32_*35del | |
NM_004004.6:c.*32_*35del MANE Select | NP_003995.2:n.*32_*35del |