HGVS | Genome Assembly |
---|---|
NC_000005.10:g.80675017_80675022del , CM000667.2:g.80675017_80675022del | GRCh38 |
NC_000005.9:g.79970836_79970841del , CM000667.1:g.79970836_79970841del | GRCh37 |
NC_000005.8:g.80006592_80006597del | NCBI36 |
NG_016607.1:g.25543_25548del | |
NG_016607.2:g.25543_25548del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265081.7:c.1062_1067del MANE Select | ENSP00000265081.6:p.Asn355_Val356del | |
ENST00000658259.1:c.894_899del | ENSP00000499617.1:p.Asn299_Val300del | |
ENST00000667069.1:c.1062_1067del | ENSP00000499502.1:p.Asn355_Val356del | |
ENST00000670357.1:c.1062_1067del | ENSP00000499791.1:p.Asn355_Val356del | |
ENST00000265081.6:c.1062_1067del | ENSP00000265081.6:p.Asn355_Val356del | |
NM_002439.4:c.1062_1067del | NP_002430.3:p.Asn355_Val356del | |
NM_002439.5:c.1062_1067del MANE Select | NP_002430.3:p.Asn355_Val356del |