HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990510_45990511insTCTTA , CM000683.2:g.45990510_45990511insTCTTA | GRCh38 |
NC_000021.8:g.47410424_47410425insTCTTA , CM000683.1:g.47410424_47410425insTCTTA | GRCh37 |
NC_000021.7:g.46234852_46234853insTCTTA | NCBI36 |
NG_008674.1:g.13762_13763insTCTTA , LRG_475:g.13762_13763insTCTTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+88_1002+89insTCTTA MANE Select | ENSP00000355180.3:n.1002+88_1002+89insTCTTA | |
ENST00000361866.7:c.1002+88_1002+89insTCTTA | ENSP00000355180.3:n.1002+88_1002+89insTCTTA | |
ENST00000612273.1:c.1002+88_1002+89insTCTTA | ENSP00000483630.1:n.1002+88_1002+89insTCTTA | |
NM_001848.2:c.1002+88_1002+89insTCTTA , LRG_475t1:c.1002+88_1002+89insTCTTA | NP_001839.2:n.1002+88_1002+89insTCTTA | |
NM_001848.3:c.1002+88_1002+89insTCTTA MANE Select | NP_001839.2:n.1002+88_1002+89insTCTTA |