HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65246895_65246896insCAA , CM000674.2:g.65246895_65246896insCAA | GRCh38 |
NC_000012.11:g.65640675_65640676insCAA , CM000674.1:g.65640675_65640676insCAA | GRCh37 |
NC_000012.10:g.63926942_63926943insCAA | NCBI36 |
NG_016210.1:g.82325_82326insCAA | |
NG_016210.2:g.82325_82326insCAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.*570_*571insCAA MANE Select | ENSP00000308369.2:n.*570_*571insCAA | |
ENST00000308330.2:c.*570_*571insCAA | ENSP00000308369.2:n.*570_*571insCAA | |
NM_001167614.1:c.*570_*571insCAA | NP_001161086.1:n.*570_*571insCAA | |
NM_014319.4:c.*570_*571insCAA | NP_055134.2:n.*570_*571insCAA | |
NM_014319.5:c.*570_*571insCAA MANE Select | NP_055134.2:n.*570_*571insCAA | |
NM_001167614.2:c.*570_*571insCAA | NP_001161086.1:n.*570_*571insCAA |