HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7530188_7530232del , CM000681.2:g.7530188_7530232del | GRCh38 |
NC_000019.9:g.7595074_7595118del , CM000681.1:g.7595074_7595118del | GRCh37 |
NC_000019.8:g.7501074_7501118del | NCBI36 |
NG_013374.1:g.1037_1081del | |
NG_015806.1:g.12579_12623del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.1360-98_1360-54del MANE Select | ENSP00000264079.5:n.1360-98_1360-54del | |
ENST00000264079.10:c.1360-98_1360-54del | ENSP00000264079.5:n.1360-98_1360-54del | |
ENST00000394321.9:n.1675-98_1675-54del | ||
ENST00000594692.1:n.356-98_356-54del | ||
ENST00000595860.5:n.543-98_543-54del | ||
ENST00000599334.1:c.237-247_237-203del | ||
NM_020533.2:c.1360-98_1360-54del | NP_065394.1:n.1360-98_1360-54del | |
NM_020533.3:c.1360-98_1360-54del MANE Select | NP_065394.1:n.1360-98_1360-54del |