HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152310913_152310972dup , CM000663.2:g.152310913_152310972dup | GRCh38 |
NC_000001.10:g.152283389_152283448dup , CM000663.1:g.152283389_152283448dup | GRCh37 |
NC_000001.9:g.150550013_150550072dup | NCBI36 |
NG_016190.1:g.19242_19301dup , LRG_1028:g.19242_19301dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368799.2:c.3924_3983dup MANE Select | ENSP00000357789.1:p.Arg1327_Gln1328insHis... | |
ENST00000368799.1:c.3924_3983dup | ENSP00000357789.1:p.Arg1327_Gln1328insHis... | |
NM_002016.1:c.3924_3983dup , LRG_1028t1:c.3924_3983dup | NP_002007.1:p.Arg1327_Gln1328insHisProGly... | |
XM_011509329.1:c.3924_3983dup | XP_011507631.1:p.Arg1327_Gln1328insHisPro... | |
NM_002016.2:c.3924_3983dup MANE Select | NP_002007.1:p.Arg1327_Gln1328insHisProGly... |