HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29071136_29071162dup , CM000664.2:g.29071136_29071162dup | GRCh38 |
NC_000002.11:g.29294002_29294028dup , CM000664.1:g.29294002_29294028dup | GRCh37 |
NC_000002.10:g.29147506_29147532dup | NCBI36 |
NG_021427.1:g.8100_8126dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000331664.6:c.3100_3126dup MANE Select | ENSP00000332809.4:p.Pro1042_Thr1043insVal... | |
ENST00000331664.5:c.3100_3126dup | ENSP00000332809.4:p.Pro1042_Thr1043insVal... | |
NM_001029883.2:c.3100_3126dup | NP_001025054.1:p.Pro1042_Thr1043insValSer... | |
XM_011532826.1:c.3100_3126dup | XP_011531128.1:p.Pro1042_Thr1043insValSer... | |
XR_939901.1:n.185+1969_185+1995dup | ||
XR_939902.1:n.173+1981_173+2007dup | ||
NM_001029883.3:c.3100_3126dup MANE Select | NP_001025054.1:p.Pro1042_Thr1043insValSer... |