HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94409371_94409388dup , CM000669.2:g.94409371_94409388dup | GRCh38 |
NC_000007.13:g.94038683_94038700dup , CM000669.1:g.94038683_94038700dup | GRCh37 |
NC_000007.12:g.93876619_93876636dup | NCBI36 |
NG_007405.1:g.19811_19828dup , LRG_2:g.19811_19828dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.842_859dup MANE Select | ENSP00000297268.6:p.Gly286_Leu287insProAr... | |
ENST00000297268.10:c.842_859dup | ENSP00000297268.6:p.Gly286_Leu287insProAr... | |
ENST00000620463.1:c.836_853dup | ENSP00000477719.1:p.Gly284_Leu285insProAr... | |
NM_000089.3:c.842_859dup , LRG_2t1:c.842_859dup | NP_000080.2:p.Gly286_Leu287insProArgGlyGl... | |
NM_000089.4:c.842_859dup MANE Select | NP_000080.2:p.Gly286_Leu287insProArgGlyGl... |