HGVS | Genome Assembly |
---|---|
NC_000016.10:g.23211505_23211509delinsCAGTT , CM000678.2:g.23211505_23211509delinsCAGTT | GRCh38 |
NC_000016.9:g.23222826_23222830delinsCAGTT , CM000678.1:g.23222826_23222830delinsCAGTT | GRCh37 |
NC_000016.8:g.23130327_23130331delinsCAGTT | NCBI36 |
NG_011909.1:g.33787_33791delinsCAGTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000300061.3:c.1177-529_1177-525delinsCAGTT MANE Select | ENSP00000300061.2:n.1177-529_1177-525delinsCAGTT | |
ENST00000300061.2:c.1177-529_1177-525delinsCAGTT | ENSP00000300061.2:n.1177-529_1177-525delinsCAGTT | |
NM_001039.3:c.1177-529_1177-525delinsCAGTT | NP_001030.2:n.1177-529_1177-525delinsCAGTT | |
NM_001039.4:c.1177-529_1177-525delinsCAGTT MANE Select | NP_001030.2:n.1177-529_1177-525delinsCAGTT |