HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7527788_7527789insCCCT , CM000681.2:g.7527788_7527789insCCCT | GRCh38 |
NC_000019.9:g.7592674_7592675insCCCT , CM000681.1:g.7592674_7592675insCCCT | GRCh37 |
NC_000019.8:g.7498674_7498675insCCCT | NCBI36 |
NG_015806.1:g.10179_10180insCCCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.681-76_681-75insCCCT MANE Select | ENSP00000264079.5:n.681-76_681-75insCCCT | |
ENST00000264079.10:c.681-76_681-75insCCCT | ENSP00000264079.5:n.681-76_681-75insCCCT | |
ENST00000394321.9:n.920_921insCCCT | ||
ENST00000601003.1:c.572-76_572-75insCCCT | ENSP00000469074.1:n.572-76_572-75insCCCT | |
NM_020533.2:c.681-76_681-75insCCCT | NP_065394.1:n.681-76_681-75insCCCT | |
NM_020533.3:c.681-76_681-75insCCCT MANE Select | NP_065394.1:n.681-76_681-75insCCCT |