HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160139540_160139579dup , CM000663.2:g.160139540_160139579dup | GRCh38 |
NC_000001.10:g.160109330_160109369dup , CM000663.1:g.160109330_160109369dup | GRCh37 |
NC_000001.9:g.158375954_158375993dup | NCBI36 |
NG_008014.1:g.28783_28822dup , LRG_6:g.28783_28822dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361216.8:c.2841-100_2841-61dup MANE Select | ENSP00000354490.3:n.2841-100_2841-61dup | |
ENST00000361216.7:c.2841-100_2841-61dup | ENSP00000354490.3:n.2841-100_2841-61dup | |
ENST00000392233.7:c.2841-100_2841-61dup | ENSP00000376066.3:n.2841-100_2841-61dup | |
ENST00000447527.1:c.1922-100_1922-61dup | ||
ENST00000463989.1:n.177-100_177-61dup | ||
NM_000702.3:c.2841-100_2841-61dup | NP_000693.1:n.2841-100_2841-61dup | |
NM_000702.4:c.2841-100_2841-61dup MANE Select | NP_000693.1:n.2841-100_2841-61dup |