HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29451467dup , CM000679.2:g.29451467dup | GRCh38 |
NC_000017.10:g.27778485dup , CM000679.1:g.27778485dup | GRCh37 |
NC_000017.9:g.24802611dup | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261716.8:c.-82dup MANE Select | ENSP00000261716.3:n.-82dup | |
ENST00000261716.7:c.-82dup | ENSP00000261716.3:n.-82dup | |
ENST00000536202.1:c.-82dup | ENSP00000438819.1:n.-82dup | |
ENST00000583121.5:c.-82dup | ENSP00000464562.1:n.-82dup | |
ENST00000587277.1:n.113dup | ||
NM_020791.2:c.-82dup | NP_065842.1:n.-82dup | |
NM_025142.1:c.-82dup | NP_079418.1:n.-82dup | |
XM_011525060.1:c.-82dup | XP_011523362.1:n.-82dup | |
XM_011525060.2:c.-82dup | XP_011523362.1:n.-82dup | |
NM_020791.4:c.-82dup MANE Select | NP_065842.1:n.-82dup |