HGVS | Genome Assembly |
---|---|
NC_000022.11:g.39244732_39244739delinsGGCTGCGA , CM000684.2:g.39244732_39244739delinsGGCTGCGA | GRCh38 |
NC_000022.10:g.39640737_39640744delinsGGCTGCGA , CM000684.1:g.39640737_39640744delinsGGCTGCGA | GRCh37 |
NC_000022.9:g.37970683_37970690delinsGGCTGCGA | NCBI36 |
NG_012111.1:g.5214_5221delinsTCGCAGCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331163.11:c.-776_-769delinsTCGCAGCC MANE Select | ENSP00000330382.6:n.-776_-769delinsTCGCAGCC | |
ENST00000331163.10:c.-776_-769delinsTCGCAGCC | ENSP00000330382.6:n.-776_-769delinsTCGCAGCC | |
NM_002608.2:c.-776_-769delinsTCGCAGCC | NP_002599.1:n.-776_-769delinsTCGCAGCC | |
NM_002608.3:c.-776_-769delinsTCGCAGCC | NP_002599.1:n.-776_-769delinsTCGCAGCC | |
NM_002608.4:c.-776_-769delinsTCGCAGCC MANE Select | NP_002599.1:n.-776_-769delinsTCGCAGCC |