HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202599_32202600insACAACCAAA , CM000668.2:g.32202599_32202600insACAACCAAA | GRCh38 |
NC_000006.11:g.32170376_32170377insACAACCAAA , CM000668.1:g.32170376_32170377insACAACCAAA | GRCh37 |
NC_000006.10:g.32278354_32278355insACAACCAAA | NCBI36 |
NG_028190.1:g.26468_26469insTTTGGTTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-1_3232insTTTGGTTGT MANE Select | ENSP00000364163.3:n.3232-1_3232insTTTGGTTGT | |
ENST00000474612.1:n.1317_1318insTTTGGTTGT | ||
NM_004557.3:c.3232-1_3232insTTTGGTTGT | NP_004548.3:n.3232-1_3232insTTTGGTTGT | |
NR_134949.1:n.3473-1100_3473-1099insTTTGGTTGT | ||
NR_134950.1:n.3371-1100_3371-1099insTTTGGTTGT | ||
NM_004557.4:c.3232-1_3232insTTTGGTTGT MANE Select | NP_004548.3:n.3232-1_3232insTTTGGTTGT | |
NR_134949.2:n.3473-1100_3473-1099insTTTGGTTGT | ||
NR_134950.2:n.3371-1100_3371-1099insTTTGGTTGT |