HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663148_36663154dup , CM000676.2:g.36663148_36663154dup | GRCh38 |
NC_000014.8:g.37132353_37132359dup , CM000676.1:g.37132353_37132359dup | GRCh37 |
NC_000014.7:g.36202104_36202110dup | NCBI36 |
NG_013357.1:g.10581_10587dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.256_262dup MANE Select | ENSP00000355245.6:p.Arg88ProfsTer? | |
ENST00000361487.6:c.256_262dup | ENSP00000355245.6:p.Arg88ProfsTer? | |
ENST00000402703.6:c.256_262dup | ENSP00000384817.2:p.Arg88ProfsTer? | |
ENST00000554201.1:c.-306_-300dup | ENSP00000450434.1:n.-306_-300dup | |
NM_006194.3:c.256_262dup | NP_006185.1:p.Arg88ProfsTer? | |
NM_001372076.1:c.256_262dup MANE Select | NP_001359005.1:p.Arg88ProfsTer? | |
NM_006194.4:c.256_262dup | NP_006185.1:p.Arg88ProfsTer? |