HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58782451_58782456dup , CM000663.2:g.58782451_58782456dup | GRCh38 |
NC_000001.10:g.59248123_59248128dup , CM000663.1:g.59248123_59248128dup | GRCh37 |
NC_000001.9:g.59020711_59020716dup | NCBI36 |
NG_047027.1:g.6660_6665dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000710273.1:c.683_688dup | ENSP00000518166.1:p.Pro229_Pro230insGlnPro | |
ENST00000371222.4:c.617_622dup MANE Select | ENSP00000360266.2:p.Pro207_Pro208insGlnPro | |
ENST00000678696.1:c.617_622dup | ENSP00000503132.1:p.Pro207_Pro208insGlnPro | |
ENST00000371222.3:c.617_622dup | ENSP00000360266.2:p.Pro207_Pro208insGlnPro | |
NM_002228.3:c.617_622dup | NP_002219.1:p.Pro207_Pro208insGlnPro | |
NM_002228.4:c.617_622dup MANE Select | NP_002219.1:p.Pro207_Pro208insGlnPro |