HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48537790_48537793delinsCATG , CM000677.2:g.48537790_48537793delinsCATG | GRCh38 |
NC_000015.9:g.48829987_48829990delinsCATG , CM000677.1:g.48829987_48829990delinsCATG | GRCh37 |
NC_000015.8:g.46617279_46617282delinsCATG | NCBI36 |
NG_008805.2:g.112996_112999delinsCATG , LRG_778:g.112996_112999delinsCATG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.554_557delinsCATG | ENSP00000453958.2:p.Pro185= | |
ENST00000674301.2:c.554_557delinsCATG | ENSP00000501333.2:p.Pro185= | |
ENST00000316623.10:c.554_557delinsCATG MANE Select | ENSP00000325527.5:p.Pro185= | |
ENST00000316623.9:c.554_557delinsCATG | ENSP00000325527.5:p.Pro185= | |
ENST00000537463.6:c.554_557delinsCATG | ENSP00000440294.2:p.Pro185= | |
NM_000138.4:c.554_557delinsCATG , LRG_778t1:c.554_557delinsCATG | NP_000129.3:p.Pro185= | |
NM_000138.5:c.554_557delinsCATG MANE Select | NP_000129.3:p.Pro185= |