HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957721_19957725delinsTCTGA , CM000670.2:g.19957721_19957725delinsTCTGA | GRCh38 |
NC_000008.10:g.19815232_19815236delinsTCTGA , CM000670.1:g.19815232_19815236delinsTCTGA | GRCh37 |
NC_000008.9:g.19859512_19859516delinsTCTGA | NCBI36 |
NG_008855.1:g.23651_23655delinsTCTGA | |
NG_008855.2:g.61005_61009delinsTCTGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1019-1539_1019-1535delinsTCTGA MANE Select | ENSP00000497642.1:n.1019-1539_1019-1535de... | |
ENST00000650478.1:c.79+1638_79+1642delinsTCTGA | ENSP00000497560.1:n.79+1638_79+1642delins... | |
ENST00000311322.8:c.1019-1539_1019-1535delinsTCTGA | ENSP00000309757.6:n.1019-1539_1019-1535de... | |
NM_000237.2:c.1019-1539_1019-1535delinsTCTGA | NP_000228.1:n.1019-1539_1019-1535delinsTC... | |
NM_000237.3:c.1019-1539_1019-1535delinsTCTGA MANE Select | NP_000228.1:n.1019-1539_1019-1535delinsTC... |