HGVS | Genome Assembly |
---|---|
NC_000003.12:g.29167564_29167568delinsCTCTT , CM000665.2:g.29167564_29167568delinsCTCTT | GRCh38 |
NC_000003.11:g.29209055_29209059delinsCTCTT , CM000665.1:g.29209055_29209059delinsCTCTT | GRCh37 |
NC_000003.10:g.29184059_29184063delinsCTCTT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000635992.1:c.*409-15392_*409-15388delinsCTCTT | ENSP00000489994.1:n.*409-15392_*409-15388... | |
ENST00000636582.1:n.353-15392_353-15388delinsCTCTT | ||
ENST00000636680.2:c.283-15392_283-15388delinsCTCTT | ENSP00000490271.2:n.283-15392_283-15388de... | |
ENST00000636900.1:n.239-15392_239-15388delinsCTCTT | ||
ENST00000637842.1:c.149-15392_149-15388delinsCTCTT | ENSP00000489718.1:n.149-15392_149-15388de... |