HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652452_171652453insTC , CM000663.2:g.171652452_171652453insTC | GRCh38 |
NC_000001.10:g.171621592_171621593insTC , CM000663.1:g.171621592_171621593insTC | GRCh37 |
NC_000001.9:g.169888215_169888216insTC | NCBI36 |
NG_008859.1:g.5182_5183insAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.160_161insAG MANE Select | ENSP00000037502.5:p.Ala54GlufsTer31 | |
ENST00000638471.1:c.130+30_130+31insAG | ENSP00000491206.1:n.130+30_130+31insAG | |
ENST00000037502.10:c.160_161insAG | ENSP00000037502.5:p.Ala54GlufsTer31 | |
ENST00000614688.1:c.160_161insAG | ENSP00000478680.1:p.Ala54GlufsTer31 | |
NM_000261.1:c.160_161insAG | NP_000252.1:p.Ala54GlufsTer31 | |
NM_000261.2:c.160_161insAG MANE Select | NP_000252.1:p.Ala54GlufsTer31 |