HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1395020_1395023delinsTGGC , CM000667.2:g.1395020_1395023delinsTGGC | GRCh38 |
NC_000005.9:g.1395135_1395138delinsTGGC , CM000667.1:g.1395135_1395138delinsTGGC | GRCh37 |
NC_000005.8:g.1448135_1448138delinsTGGC | NCBI36 |
NG_015885.1:g.55406_55409delinsGCCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1840-265_1840-262delinsGCCA MANE Select | ENSP00000270349.9:n.1840-265_1840-262delinsGCCA | |
ENST00000270349.11:c.1840-265_1840-262delinsGCCA | ENSP00000270349.9:n.1840-265_1840-262delinsGCCA | |
ENST00000512002.2:n.221-265_221-262delinsGCCA | ||
NM_001044.4:c.1840-265_1840-262delinsGCCA | NP_001035.1:n.1840-265_1840-262delinsGCCA | |
NM_001044.5:c.1840-265_1840-262delinsGCCA MANE Select | NP_001035.1:n.1840-265_1840-262delinsGCCA |