HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551900_43551905del , CM000681.2:g.43551900_43551905del | GRCh38 |
NC_000019.9:g.44056052_44056057del , CM000681.1:g.44056052_44056057del | GRCh37 |
NC_000019.8:g.48747892_48747897del | NCBI36 |
NG_033799.1:g.28674_28679del , LRG_784:g.28674_28679del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1082+112_1082+117del MANE Select | ENSP00000262887.5:n.1082+112_1082+117del | |
ENST00000262887.9:c.1082+112_1082+117del | ENSP00000262887.4:n.1082+112_1082+117del | |
ENST00000543982.5:c.989+112_989+117del | ENSP00000443671.1:n.989+112_989+117del | |
ENST00000597811.5:c.692+112_692+117del | ||
NM_006297.2:c.1082+112_1082+117del , LRG_784t1:c.1082+112_1082+117del | NP_006288.2:n.1082+112_1082+117del | |
NM_006297.3:c.1082+112_1082+117del MANE Select | NP_006288.2:n.1082+112_1082+117del |