HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551897_43551898insT , CM000681.2:g.43551897_43551898insT | GRCh38 |
NC_000019.9:g.44056049_44056050insT , CM000681.1:g.44056049_44056050insT | GRCh37 |
NC_000019.8:g.48747889_48747890insT | NCBI36 |
NG_033799.1:g.28681_28682insA , LRG_784:g.28681_28682insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1082+119_1082+120insA MANE Select | ENSP00000262887.5:n.1082+119_1082+120insA | |
ENST00000262887.9:c.1082+119_1082+120insA | ENSP00000262887.4:n.1082+119_1082+120insA | |
ENST00000543982.5:c.989+119_989+120insA | ENSP00000443671.1:n.989+119_989+120insA | |
ENST00000597811.5:c.692+119_692+120insA | ||
NM_006297.2:c.1082+119_1082+120insA , LRG_784t1:c.1082+119_1082+120insA | NP_006288.2:n.1082+119_1082+120insA | |
NM_006297.3:c.1082+119_1082+120insA MANE Select | NP_006288.2:n.1082+119_1082+120insA |