HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8732011_8732019del , CM000685.2:g.8732011_8732019del | GRCh38 |
NC_000023.10:g.8700052_8700060del , CM000685.1:g.8700052_8700060del | GRCh37 |
NC_000023.9:g.8660052_8660060del | NCBI36 |
NG_007088.1:g.5169_5177del | |
NG_007088.2:g.5169_5177del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.19_27del MANE Select | ENSP00000262648.3:p.Gly7_Val9del | |
ENST00000262648.7:c.19_27del | ENSP00000262648.3:p.Gly7_Val9del | |
ENST00000619786.1:c.19_27del | ENSP00000478734.1:p.Gly7_Val9del | |
NM_000216.2:c.19_27del | NP_000207.2:p.Gly7_Val9del | |
XM_005274501.3:c.19_27del | XP_005274558.1:p.Gly7_Val9del | |
NM_000216.3:c.19_27del | NP_000207.2:p.Gly7_Val9del | |
XM_005274501.4:c.19_27del | XP_005274558.1:p.Gly7_Val9del | |
NM_000216.4:c.19_27del MANE Select | NP_000207.2:p.Gly7_Val9del |