HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551764_43551765del , CM000681.2:g.43551764_43551765del | GRCh38 |
NC_000019.9:g.44055916_44055917del , CM000681.1:g.44055916_44055917del | GRCh37 |
NC_000019.8:g.48747756_48747757del | NCBI36 |
NG_033799.1:g.28815_28816del , LRG_784:g.28815_28816del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1083-77_1083-76del MANE Select | ENSP00000262887.5:n.1083-77_1083-76del | |
ENST00000262887.9:c.1083-77_1083-76del | ENSP00000262887.4:n.1083-77_1083-76del | |
ENST00000543982.5:c.990-77_990-76del | ENSP00000443671.1:n.990-77_990-76del | |
ENST00000597811.5:c.693-77_693-76del | ||
NM_006297.2:c.1083-77_1083-76del , LRG_784t1:c.1083-77_1083-76del | NP_006288.2:n.1083-77_1083-76del | |
NM_006297.3:c.1083-77_1083-76del MANE Select | NP_006288.2:n.1083-77_1083-76del |