HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94775182_94775184delinsGCC , CM000672.2:g.94775182_94775184delinsGCC | GRCh38 |
NC_000010.10:g.96534939_96534941delinsGCC , CM000672.1:g.96534939_96534941delinsGCC | GRCh37 |
NC_000010.9:g.96524929_96524931delinsGCC | NCBI36 |
NG_008384.2:g.17477_17479delinsGCC | |
NG_008384.3:g.17502_17504delinsGCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.293_295delinsGCC MANE Select | ENSP00000360372.3:p.Gly98= | |
ENST00000645461.1:n.1346_1348delinsGCC | ||
ENST00000371321.7:c.293_295delinsGCC | ENSP00000360372.3:p.Gly98= | |
ENST00000464755.1:c.1056_1058delinsGCC | ENSP00000483243.1:n.1056_1058delinsGCC | |
ENST00000480405.2:c.293_295delinsGCC | ENSP00000483847.1:p.Gly98= | |
NM_000769.2:c.293_295delinsGCC | NP_000760.1:p.Gly98= | |
NM_000769.4:c.293_295delinsGCC MANE Select | NP_000760.1:p.Gly98= |