HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6058135_6058137del , CM000674.2:g.6058135_6058137del | GRCh38 |
NC_000012.11:g.6167301_6167303del , CM000674.1:g.6167301_6167303del | GRCh37 |
NC_000012.10:g.6037562_6037564del | NCBI36 |
NG_009072.1:g.71543_71545del | |
NG_009072.2:g.71543_71545del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.1534-84_1534-82del MANE Select | ENSP00000261405.5:n.1534-84_1534-82del | |
ENST00000261405.9:c.1534-84_1534-82del | ENSP00000261405.5:n.1534-84_1534-82del | |
ENST00000538635.5:n.420+52387_420+52389del | ||
NM_000552.3:c.1534-84_1534-82del | NP_000543.2:n.1534-84_1534-82del | |
NM_000552.4:c.1534-84_1534-82del | NP_000543.2:n.1534-84_1534-82del | |
NM_000552.5:c.1534-84_1534-82del MANE Select | NP_000543.3:n.1534-84_1534-82del |