HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110911004_110911005insGTGTT , CM000674.2:g.110911004_110911005insGTGTT | GRCh38 |
NC_000012.11:g.111348808_111348809insGTGTT , CM000674.1:g.111348808_111348809insGTGTT | GRCh37 |
NC_000012.10:g.109833191_109833192insGTGTT | NCBI36 |
NG_007554.1:g.14574_14575insACACA , LRG_393:g.14574_14575insACACA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.*73_*74insACACA MANE Select | ENSP00000228841.8:n.*73_*74insACACA | |
ENST00000663220.1:c.*73_*74insACACA | ENSP00000499568.1:n.*73_*74insACACA | |
ENST00000228841.12:c.*73_*74insACACA | ENSP00000228841.7:n.*73_*74insACACA | |
ENST00000548438.1:c.*73_*74insACACA | ENSP00000447154.1:n.*73_*74insACACA | |
NM_000432.3:c.*73_*74insACACA , LRG_393t1:c.*73_*74insACACA | NP_000423.2:n.*73_*74insACACA | |
NM_000432.4:c.*73_*74insACACA MANE Select | NP_000423.2:n.*73_*74insACACA |