HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256347_133256348delinsAG , CM000671.2:g.133256347_133256348delinsAG | GRCh38 |
NC_000009.11:g.136131734_136131735delinsAG , CM000671.1:g.136131734_136131735delinsAG | GRCh37 |
NC_000009.10:g.135121555_135121556delinsAG | NCBI36 |
NG_006669.1:g.21320_21321delinsCT | |
NG_006669.2:g.23868_23869delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.412_413delinsCT | ||
ENST00000647353.1:n.54-5196_54-5195delinsCT | ||
ENST00000651471.1:n.338_339delinsCT | ||
ENST00000679909.1:c.28+18814_28+18815delinsCT | ENSP00000506089.1:n.28+18814_28+18815delinsCT | |
ENST00000453660.3:n.394_395delinsCT | ||
ENST00000538324.2:c.380_381delinsCT | ENSP00000483018.1:p.Ala127= | |
ENST00000611156.4:c.380_381delinsCT | ENSP00000483265.1:p.Ala127= | |
NM_020469.2:c.383_384delinsCT | NP_065202.2:p.Ala128= | |
NM_020469.3:c.383_384delinsCT | NP_065202.2:p.Ala128= |