HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813816dup , CM000671.2:g.129813816dup | GRCh38 |
NC_000009.11:g.132576095dup , CM000671.1:g.132576095dup | GRCh37 |
NC_000009.10:g.131615916dup | NCBI36 |
NG_008049.1:g.15351dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*160dup MANE Select | ENSP00000345719.4:n.*160dup | |
ENST00000651202.1:c.*427dup | ENSP00000498222.1:n.*427dup | |
ENST00000351698.4:c.*160dup | ENSP00000345719.4:n.*160dup | |
ENST00000474192.1:n.743dup | ||
NM_000113.2:c.*160dup | NP_000104.1:n.*160dup | |
XR_929731.3:n.1354dup | ||
NM_000113.3:c.*160dup MANE Select | NP_000104.1:n.*160dup |