HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942307_94942309delinsCCG , CM000672.2:g.94942307_94942309delinsCCG | GRCh38 |
NC_000010.10:g.96702064_96702066delinsCCG , CM000672.1:g.96702064_96702066delinsCCG | GRCh37 |
NC_000010.9:g.96692054_96692056delinsCCG | NCBI36 |
NG_008385.1:g.8650_8652delinsCCG | |
NG_008385.2:g.9150_9152delinsCCG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.447_449delinsCCG MANE Select | ENSP00000260682.6:p.Ala149= | |
ENST00000643112.1:c.447_449delinsCCG | ENSP00000496202.1:p.Ala149= | |
ENST00000645207.1:n.600_602delinsCCG | ||
ENST00000260682.6:c.447_449delinsCCG | ENSP00000260682.6:p.Ala149= | |
ENST00000461906.1:n.472_474delinsCCG | ||
ENST00000473496.1:n.218_220delinsCCG | ||
NM_000771.3:c.447_449delinsCCG | NP_000762.2:p.Ala149= | |
NM_000771.4:c.447_449delinsCCG MANE Select | NP_000762.2:p.Ala149= |