HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47284683_47284684delinsAC , CM000679.2:g.47284683_47284684delinsAC | GRCh38 |
NC_000017.10:g.45362049_45362050delinsAC , CM000679.1:g.45362049_45362050delinsAC | GRCh37 |
NC_000017.9:g.42717048_42717049delinsAC | NCBI36 |
NG_008332.2:g.35842_35843delinsAC , LRG_481:g.35842_35843delinsAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.602_603delinsAC | ENSP00000513002.1:p.Asn201= | |
ENST00000559488.7:c.602_603delinsAC MANE Select | ENSP00000452786.2:p.Asn201= | |
ENST00000559488.5:c.602_603delinsAC | ENSP00000452786.1:p.Asn201= | |
ENST00000560629.1:c.567_568delinsAC | ||
ENST00000571680.1:c.602_603delinsAC | ENSP00000461626.1:p.Asn201= | |
NM_000212.2:c.602_603delinsAC , LRG_481t1:c.602_603delinsAC | NP_000203.2:p.Asn201= | |
NM_000212.3:c.602_603delinsAC MANE Select | NP_000203.2:p.Asn201= |