HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169572587_169572602dup , CM000663.2:g.169572587_169572602dup | GRCh38 |
NC_000001.10:g.169541825_169541840dup , CM000663.1:g.169541825_169541840dup | GRCh37 |
NC_000001.9:g.167808449_167808464dup | NCBI36 |
NG_011806.1:g.18930_18945dup , LRG_553:g.18930_18945dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.251-259_251-244dup MANE Select | ENSP00000356771.3:n.251-259_251-244dup | |
ENST00000367796.3:c.251-259_251-244dup | ENSP00000356770.3:n.251-259_251-244dup | |
ENST00000367797.7:c.251-259_251-244dup | ENSP00000356771.3:n.251-259_251-244dup | |
NM_000130.4:c.251-259_251-244dup , LRG_553t1:c.251-259_251-244dup | NP_000121.2:n.251-259_251-244dup | |
XM_017000660.2:c.-161-259_-161-244dup | XP_016856149.1:n.-161-259_-161-244dup | |
NM_000130.5:c.251-259_251-244dup MANE Select | NP_000121.2:n.251-259_251-244dup |