HGVS | Genome Assembly |
---|---|
NC_000005.10:g.178994859_178994876dup , CM000667.2:g.178994859_178994876dup | GRCh38 |
NC_000005.9:g.178421860_178421877dup , CM000667.1:g.178421860_178421877dup | GRCh37 |
NC_000005.8:g.178354466_178354483dup | NCBI36 |
NG_008105.1:g.5255_5272dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517717.3:c.76_93dup MANE Select | ENSP00000430767.1:p.Gly31_Ser32insLeuAlaArgAlaAlaGly | |
ENST00000650031.1:c.76_93dup | ENSP00000497110.1:p.Gly31_Ser32insLeuAlaArgAlaAlaGly | |
ENST00000231188.9:c.76_93dup | ENSP00000231188.5:p.Gly31_Ser32insLeuAlaArgAlaAlaGly | |
ENST00000517717.1:c.76_93dup | ENSP00000430767.1:p.Gly31_Ser32insLeuAlaArgAlaAlaGly | |
NM_000843.3:c.76_93dup | NP_000834.2:p.Gly31_Ser32insLeuAlaArgAlaAlaGly | |
NM_000843.4:c.76_93dup MANE Select | NP_000834.2:p.Gly31_Ser32insLeuAlaArgAlaAlaGly |