HGVS | Genome Assembly |
---|---|
NC_000007.14:g.100647169_100647170insCA , CM000669.2:g.100647169_100647170insCA | GRCh38 |
NC_000007.13:g.100244792_100244793insCA , CM000669.1:g.100244792_100244793insCA | GRCh37 |
NC_000007.12:g.100082728_100082729insCA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000160382.10:c.821+53_821+54insTG MANE Select | ENSP00000160382.5:n.821+53_821+54insTG | |
ENST00000160382.9:c.821+53_821+54insTG | ENSP00000160382.5:n.821+53_821+54insTG | |
ENST00000487125.1:n.357+53_357+54insTG | ||
NM_016188.4:c.821+53_821+54insTG | NP_057272.1:n.821+53_821+54insTG | |
XR_927476.1:n.928+53_928+54insTG | ||
NR_134539.1:n.928+53_928+54insTG | ||
NM_016188.5:c.821+53_821+54insTG MANE Select | NP_057272.1:n.821+53_821+54insTG | |
NR_134539.2:n.915+53_915+54insTG |