HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571700_154571708del , CM000663.2:g.154571700_154571708del | GRCh38 |
NC_000001.10:g.154544176_154544184del , CM000663.1:g.154544176_154544184del | GRCh37 |
NC_000001.9:g.152810800_152810808del | NCBI36 |
NG_008027.1:g.8920_8928del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.877_885del MANE Select | ENSP00000357461.3:p.Asp293_Pro295del | |
ENST00000636034.1:c.877_885del | ENSP00000489703.1:p.Asp293_Pro295del | |
ENST00000637900.1:c.883_891del | ENSP00000490474.1:p.Asp295_Pro297del | |
ENST00000368476.3:c.877_885del | ENSP00000357461.3:p.Asp293_Pro295del | |
NM_000748.2:c.877_885del | NP_000739.1:p.Asp293_Pro295del | |
XM_017000180.2:c.367_375del | XP_016855669.1:p.Asp123_Pro125del | |
XR_001736952.2:n.1129_1137del | ||
NM_000748.3:c.877_885del MANE Select | NP_000739.1:p.Asp293_Pro295del |