HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24261691_24261692delinsTG , CM000676.2:g.24261691_24261692delinsTG | GRCh38 |
NC_000014.8:g.24730897_24730898delinsTG , CM000676.1:g.24730897_24730898delinsTG | GRCh37 |
NC_000014.7:g.23800737_23800738delinsTG | NCBI36 |
NG_007150.1:g.6475_6476delinsCA | |
NG_007150.2:g.6475_6476delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000206765.11:c.508+3_508+4delinsCA MANE Select | ENSP00000206765.6:n.508+3_508+4delinsCA | |
ENST00000206765.10:c.508+3_508+4delinsCA | ENSP00000206765.6:n.508+3_508+4delinsCA | |
ENST00000544573.5:c.-29+435_-29+436delinsCA | ENSP00000439446.1:n.-29+435_-29+436delins... | |
NM_000359.2:c.508+3_508+4delinsCA | NP_000350.1:n.508+3_508+4delinsCA | |
NM_000359.3:c.508+3_508+4delinsCA MANE Select | NP_000350.1:n.508+3_508+4delinsCA |