HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213352_1213353insTG , CM000667.2:g.1213352_1213353insTG | GRCh38 |
NC_000005.9:g.1213467_1213468insTG , CM000667.1:g.1213467_1213468insTG | GRCh37 |
NC_000005.8:g.1266467_1266468insTG | NCBI36 |
NG_008282.1:g.16758_16759insTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-111_664-110insTG MANE Select | ENSP00000305302.10:n.664-111_664-110insTG | |
ENST00000304460.10:c.664-111_664-110insTG | ENSP00000305302.10:n.664-111_664-110insTG | |
ENST00000515652.5:c.572-111_572-110insTG | ENSP00000425701.1:n.572-111_572-110insTG | |
NM_001003841.2:c.664-111_664-110insTG | NP_001003841.1:n.664-111_664-110insTG | |
NM_001003841.3:c.664-111_664-110insTG MANE Select | NP_001003841.1:n.664-111_664-110insTG |