HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78118310_78118311insCA , CM000685.2:g.78118310_78118311insCA | GRCh38 |
NC_000023.10:g.77373807_77373808insCA , CM000685.1:g.77373807_77373808insCA | GRCh37 |
NC_000023.9:g.77260463_77260464insCA | NCBI36 |
NG_008862.1:g.19142_19143insCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.641+140_641+141insCA MANE Select | ENSP00000362413.4:n.641+140_641+141insCA | |
ENST00000644362.1:c.557+140_557+141insCA | ENSP00000496140.1:n.557+140_557+141insCA | |
ENST00000373316.4:c.641+140_641+141insCA | ENSP00000362413.4:n.641+140_641+141insCA | |
ENST00000491291.1:n.633+140_633+141insCA | ||
NM_000291.3:c.641+140_641+141insCA | NP_000282.1:n.641+140_641+141insCA | |
NM_000291.4:c.641+140_641+141insCA MANE Select | NP_000282.1:n.641+140_641+141insCA |