HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443600_32443604delinsCCTTT , CM000668.2:g.32443600_32443604delinsCCTTT | GRCh38 |
NC_000006.11:g.32411377_32411381delinsCCTTT , CM000668.1:g.32411377_32411381delinsCCTTT | GRCh37 |
NC_000006.10:g.32519355_32519359delinsCCTTT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000395388.7:c.610+134_610+138delinsCCTTT MANE Select | ENSP00000378786.2:n.610+134_610+138delinsCCTTT | |
ENST00000374982.5:c.535+134_535+138delinsCCTTT | ENSP00000364121.5:n.535+134_535+138delinsCCTTT | |
ENST00000395388.6:c.610+134_610+138delinsCCTTT | ENSP00000378786.2:n.610+134_610+138delinsCCTTT | |
NM_019111.4:c.610+134_610+138delinsCCTTT | NP_061984.2:n.610+134_610+138delinsCCTTT | |
NM_019111.5:c.610+134_610+138delinsCCTTT MANE Select | NP_061984.2:n.610+134_610+138delinsCCTTT |