HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085374_186085375delinsTC , CM000666.2:g.186085374_186085375delinsTC | GRCh38 |
NC_000004.11:g.187006528_187006529delinsTC , CM000666.1:g.187006528_187006529delinsTC | GRCh37 |
NC_000004.10:g.187243522_187243523delinsTC | NCBI36 |
NG_007278.1:g.21220_21221delinsTC , LRG_117:g.21220_21221delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2768_*2769delinsTC | ENSP00000513675.1:n.*2768_*2769delinsTC | |
ENST00000698353.1:n.3091_3092delinsTC | ||
ENST00000698354.1:c.*501_*502delinsTC | ENSP00000513676.1:n.*501_*502delinsTC | |
ENST00000296795.8:c.*501_*502delinsTC MANE Select | ENSP00000296795.3:n.*501_*502delinsTC | |
ENST00000296795.7:c.*501_*502delinsTC | ENSP00000296795.2:n.*501_*502delinsTC | |
NM_003265.3:c.*501_*502delinsTC MANE Select | NP_003256.1:n.*501_*502delinsTC |