HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32474906_32474909dup , CM000684.2:g.32474906_32474909dup | GRCh38 |
NC_000022.10:g.32870893_32870896dup , CM000684.1:g.32870893_32870896dup | GRCh37 |
NC_000022.9:g.31200893_31200896dup | NCBI36 |
NG_016001.1:g.5187_5190dup | |
NG_016001.2:g.5187_5190dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266087.12:c.-97_-94dup MANE Select | ENSP00000266087.7:n.-97_-94dup | |
ENST00000266087.11:c.-97_-94dup | ENSP00000266087.7:n.-97_-94dup | |
ENST00000420700.5:c.-97_-94dup | ENSP00000406155.1:n.-97_-94dup | |
ENST00000425028.5:c.-97_-94dup | ENSP00000395823.1:n.-97_-94dup | |
NM_012179.3:c.-97_-94dup | NP_036311.3:n.-97_-94dup | |
XM_011530106.1:c.-270_-267dup | XP_011528408.1:n.-270_-267dup | |
XM_024452207.1:c.-287_-284dup | XP_024307975.1:n.-287_-284dup | |
NM_012179.4:c.-97_-94dup MANE Select | NP_036311.3:n.-97_-94dup |