HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49447819_49447820insTT , CM000668.2:g.49447819_49447820insTT | GRCh38 |
NC_000006.11:g.49415532_49415533insTT , CM000668.1:g.49415532_49415533insTT | GRCh37 |
NC_000006.10:g.49523491_49523492insTT | NCBI36 |
NG_007100.1:g.20320_20321insAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.1445-35_1445-34insAA MANE Select | ENSP00000274813.3:n.1445-35_1445-34insAA | |
ENST00000274813.3:c.1445-35_1445-34insAA | ENSP00000274813.3:n.1445-35_1445-34insAA | |
NM_000255.3:c.1445-35_1445-34insAA | NP_000246.2:n.1445-35_1445-34insAA | |
XM_005249143.2:c.1445-35_1445-34insAA | XP_005249200.1:n.1445-35_1445-34insAA | |
XM_005249143.3:c.1445-35_1445-34insAA | XP_005249200.1:n.1445-35_1445-34insAA | |
NM_000255.4:c.1445-35_1445-34insAA MANE Select | NP_000246.2:n.1445-35_1445-34insAA |