HGVS | Genome Assembly |
---|---|
NC_000005.10:g.178994861_178994875dup , CM000667.2:g.178994861_178994875dup | GRCh38 |
NC_000005.9:g.178421862_178421876dup , CM000667.1:g.178421862_178421876dup | GRCh37 |
NC_000005.8:g.178354468_178354482dup | NCBI36 |
NG_008105.1:g.5253_5267dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517717.3:c.74_88dup MANE Select | ENSP00000430767.1:p.Ala29_Ala30insGlyLeuAlaArgAla | |
ENST00000650031.1:c.74_88dup | ENSP00000497110.1:p.Ala29_Ala30insGlyLeuAlaArgAla | |
ENST00000231188.9:c.74_88dup | ENSP00000231188.5:p.Ala29_Ala30insGlyLeuAlaArgAla | |
ENST00000517717.1:c.74_88dup | ENSP00000430767.1:p.Ala29_Ala30insGlyLeuAlaArgAla | |
NM_000843.3:c.74_88dup | NP_000834.2:p.Ala29_Ala30insGlyLeuAlaArgAla | |
NM_000843.4:c.74_88dup MANE Select | NP_000834.2:p.Ala29_Ala30insGlyLeuAlaArgAla |