HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423487_23423488insCAGAGA , CM000676.2:g.23423487_23423488insCAGAGA | GRCh38 |
NC_000014.8:g.23892696_23892697insCAGAGA , CM000676.1:g.23892696_23892697insCAGAGA | GRCh37 |
NC_000014.7:g.22962536_22962537insCAGAGA | NCBI36 |
NG_007884.1:g.17175_17176insCTCTGT , LRG_384:g.17175_17176insCTCTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+60_3099+61insCTCTGT MANE Select | ENSP00000347507.3:n.3099+60_3099+61insCTCTGT | |
ENST00000355349.3:c.3099+60_3099+61insCTCTGT | ENSP00000347507.3:n.3099+60_3099+61insCTCTGT | |
NM_000257.3:c.3099+60_3099+61insCTCTGT | NP_000248.2:n.3099+60_3099+61insCTCTGT | |
XR_245686.3:n.3205+60_3205+61insCTCTGT | ||
XM_017021340.1:c.3099+60_3099+61insCTCTGT | XP_016876829.1:n.3099+60_3099+61insCTCTGT | |
NM_000257.4:c.3099+60_3099+61insCTCTGT MANE Select | NP_000248.2:n.3099+60_3099+61insCTCTGT |