HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48410643dup , CM000677.2:g.48410643dup | GRCh38 |
NC_000015.9:g.48702840dup , CM000677.1:g.48702840dup | GRCh37 |
NC_000015.8:g.46490132dup | NCBI36 |
NG_008805.2:g.240151dup , LRG_778:g.240151dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1776dup | ENSP00000453958.2:n.*1776dup | |
ENST00000682158.1:n.2349dup | ||
ENST00000682170.1:n.3149dup | ||
ENST00000682767.1:n.2265dup | ||
ENST00000316623.10:c.*352dup MANE Select | ENSP00000325527.5:n.*352dup | |
ENST00000316623.9:c.*352dup | ENSP00000325527.5:n.*352dup | |
ENST00000559133.5:c.4337dup | ||
NM_000138.4:c.*352dup , LRG_778t1:c.*352dup | NP_000129.3:n.*352dup | |
NM_000138.5:c.*352dup MANE Select | NP_000129.3:n.*352dup |