HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7529864_7529865del , CM000681.2:g.7529864_7529865del | GRCh38 |
NC_000019.9:g.7594750_7594751del , CM000681.1:g.7594750_7594751del | GRCh37 |
NC_000019.8:g.7500750_7500751del | NCBI36 |
NG_013374.1:g.713_714del | |
NG_015806.1:g.12255_12256del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.1359+152_1359+153del MANE Select | ENSP00000264079.5:n.1359+152_1359+153del | |
ENST00000264079.10:c.1359+152_1359+153del | ENSP00000264079.5:n.1359+152_1359+153del | |
ENST00000394321.9:n.1674+152_1674+153del | ||
ENST00000594692.1:n.355+152_355+153del | ||
ENST00000595860.5:n.542+152_542+153del | ||
ENST00000599334.1:c.236+152_236+153del | ||
NM_020533.2:c.1359+152_1359+153del | NP_065394.1:n.1359+152_1359+153del | |
NM_020533.3:c.1359+152_1359+153del MANE Select | NP_065394.1:n.1359+152_1359+153del |