HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65239979_65239981del , CM000674.2:g.65239979_65239981del | GRCh38 |
NC_000012.11:g.65633759_65633761del , CM000674.1:g.65633759_65633761del | GRCh37 |
NC_000012.10:g.63920026_63920028del | NCBI36 |
NG_016210.1:g.75409_75411del | |
NG_016210.2:g.75409_75411del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000308330.3:c.1972_1974del MANE Select | ENSP00000308369.2:p.Lys658del | |
ENST00000308330.2:c.1972_1974del | ENSP00000308369.2:p.Lys658del | |
NM_001167614.1:c.1969_1971del | NP_001161086.1:p.Lys657del | |
NM_014319.4:c.1972_1974del | NP_055134.2:p.Lys658del | |
NM_014319.5:c.1972_1974del MANE Select | NP_055134.2:p.Lys658del | |
NM_001167614.2:c.1969_1971del | NP_001161086.1:p.Lys657del |