HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23419686_23419691delinsGAGAAA , CM000676.2:g.23419686_23419691delinsGAGAAA | GRCh38 |
NC_000014.8:g.23888895_23888900delinsGAGAAA , CM000676.1:g.23888895_23888900delinsGAGAAA | GRCh37 |
NC_000014.7:g.22958735_22958740delinsGAGAAA | NCBI36 |
NG_007884.1:g.20971_20976delinsTTTCTC , LRG_384:g.20971_20976delinsTTTCTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3727-82_3727-77delinsTTTCTC MANE Select | ENSP00000347507.3:n.3727-82_3727-77delinsTTTCTC | |
ENST00000355349.3:c.3727-82_3727-77delinsTTTCTC | ENSP00000347507.3:n.3727-82_3727-77delinsTTTCTC | |
NM_000257.3:c.3727-82_3727-77delinsTTTCTC | NP_000248.2:n.3727-82_3727-77delinsTTTCTC | |
XM_017021340.1:c.3727-82_3727-77delinsTTTCTC | XP_016876829.1:n.3727-82_3727-77delinsTTTCTC | |
NM_000257.4:c.3727-82_3727-77delinsTTTCTC MANE Select | NP_000248.2:n.3727-82_3727-77delinsTTTCTC |