HGVS | Genome Assembly |
---|---|
NC_000017.11:g.30248916dup , CM000679.2:g.30248916dup | GRCh38 |
NC_000017.10:g.28575934dup , CM000679.1:g.28575934dup | GRCh37 |
NC_000017.9:g.25600060dup | NCBI36 |
NG_011440.1:g.48142dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261714.11:c.*102dup MANE Select | ENSP00000261714.6:n.*102dup | |
ENST00000261714.10:c.*102dup | ENSP00000261714.6:n.*102dup | |
ENST00000578090.5:c.*1144dup | ENSP00000462353.1:n.*1144dup | |
ENST00000578795.1:n.1369dup | ||
NM_000386.3:c.*102dup | NP_000377.1:n.*102dup | |
XR_934653.1:n.701-871dup | ||
XR_934655.1:n.701-3158dup | ||
NM_000386.4:c.*102dup MANE Select | NP_000377.1:n.*102dup |