HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24261691_24261693delinsTGA , CM000676.2:g.24261691_24261693delinsTGA | GRCh38 |
NC_000014.8:g.24730897_24730899delinsTGA , CM000676.1:g.24730897_24730899delinsTGA | GRCh37 |
NC_000014.7:g.23800737_23800739delinsTGA | NCBI36 |
NG_007150.1:g.6474_6476delinsTCA | |
NG_007150.2:g.6474_6476delinsTCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000206765.11:c.508+2_508+4delinsTCA MANE Select | ENSP00000206765.6:n.508+2_508+4delinsTCA | |
ENST00000206765.10:c.508+2_508+4delinsTCA | ENSP00000206765.6:n.508+2_508+4delinsTCA | |
ENST00000544573.5:c.-29+434_-29+436delinsTCA | ENSP00000439446.1:n.-29+434_-29+436delins... | |
NM_000359.2:c.508+2_508+4delinsTCA | NP_000350.1:n.508+2_508+4delinsTCA | |
NM_000359.3:c.508+2_508+4delinsTCA MANE Select | NP_000350.1:n.508+2_508+4delinsTCA |