HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190746_204190748dup , CM000663.2:g.204190746_204190748dup | GRCh38 |
NC_000001.10:g.204159874_204159876dup , CM000663.1:g.204159874_204159876dup | GRCh37 |
NC_000001.9:g.202426497_202426499dup | NCBI36 |
NG_032151.1:g.10745_10747dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.154_156dup MANE Select | ENSP00000356162.4:p.Pro52_Cys53insPro | |
ENST00000367194.4:c.154_156dup | ENSP00000356162.4:p.Pro52_Cys53insPro | |
ENST00000625357.1:c.154_156dup | ENSP00000485957.1:p.Pro52_Cys53insPro | |
NM_002256.3:c.154_156dup | NP_002247.3:p.Pro52_Cys53insPro | |
XM_011509525.1:c.154_156dup | XP_011507827.1:p.Pro52_Cys53insPro | |
NM_002256.4:c.154_156dup MANE Select | NP_002247.3:p.Pro52_Cys53insPro |