HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085832_186085834delinsCTA , CM000666.2:g.186085832_186085834delinsCTA | GRCh38 |
NC_000004.11:g.187006986_187006988delinsCTA , CM000666.1:g.187006986_187006988delinsCTA | GRCh37 |
NC_000004.10:g.187243980_187243982delinsCTA | NCBI36 |
NG_007278.1:g.21678_21680delinsCTA , LRG_117:g.21678_21680delinsCTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3226_*3228delinsCTA | ENSP00000513675.1:n.*3226_*3228delinsCTA | |
ENST00000698353.1:n.3549_3551delinsCTA | ||
ENST00000698354.1:c.*959_*961delinsCTA | ENSP00000513676.1:n.*959_*961delinsCTA | |
ENST00000296795.8:c.*959_*961delinsCTA MANE Select | ENSP00000296795.3:n.*959_*961delinsCTA | |
ENST00000296795.7:c.*959_*961delinsCTA | ENSP00000296795.2:n.*959_*961delinsCTA | |
NM_003265.3:c.*959_*961delinsCTA MANE Select | NP_003256.1:n.*959_*961delinsCTA |