HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652048_171652049insT , CM000663.2:g.171652048_171652049insT | GRCh38 |
NC_000001.10:g.171621188_171621189insT , CM000663.1:g.171621188_171621189insT | GRCh37 |
NC_000001.9:g.169887811_169887812insT | NCBI36 |
NG_008859.1:g.5585_5586insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.563_564insA MANE Select | ENSP00000037502.5:p.Arg189ProfsTer? | |
ENST00000638471.1:c.130+433_130+434insA | ENSP00000491206.1:n.130+433_130+434insA | |
ENST00000037502.10:c.563_564insA | ENSP00000037502.5:p.Arg189ProfsTer? | |
ENST00000614688.1:c.563_564insA | ENSP00000478680.1:p.Arg189ProfsTer? | |
NM_000261.1:c.563_564insA | NP_000252.1:p.Arg189ProfsTer? | |
NM_000261.2:c.563_564insA MANE Select | NP_000252.1:p.Arg189ProfsTer? |