HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117059_19117060insTGCTGCTG , CM000669.2:g.19117059_19117060insTGCTGCTG | GRCh38 |
NC_000007.13:g.19156682_19156683insTGCTGCTG , CM000669.1:g.19156682_19156683insTGCTGCTG | GRCh37 |
NC_000007.12:g.19123207_19123208insTGCTGCTG | NCBI36 |
NG_008114.1:g.5613_5614insCAGCAGCA | |
NG_008114.2:g.5613_5614insCAGCAGCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.262_263insCAGCAGCA MANE Select | ENSP00000242261.5:p.Gly88AlafsTer? | |
ENST00000242261.5:c.262_263insCAGCAGCA | ENSP00000242261.5:p.Gly88AlafsTer? | |
ENST00000354571.5:c.59_60insCAGCAGCA | ||
NM_000474.3:c.262_263insCAGCAGCA | NP_000465.1:p.Gly88AlafsTer? | |
XM_011515496.1:c.262_263insCAGCAGCA | XP_011513798.1:p.Gly88AlafsTer? | |
NR_149001.1:n.613_614insCAGCAGCA | ||
NM_000474.4:c.262_263insCAGCAGCA MANE Select | NP_000465.1:p.Gly88AlafsTer? | |
NR_149001.2:n.577_578insCAGCAGCA |