HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119651773_119651781delinsAGACCGGCT , CM000672.2:g.119651773_119651781delinsAGACCGGCT | GRCh38 |
NC_000010.10:g.121411285_121411293delinsAGACCGGCT , CM000672.1:g.121411285_121411293delinsAGACCGGCT | GRCh37 |
NC_000010.9:g.121401275_121401283delinsAGACCGGCT | NCBI36 |
NG_016125.1:g.5404_5412delinsAGACCGGCT , LRG_742:g.5404_5412delinsAGACCGGCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369085.8:c.98_106delinsAGACCGGCT MANE Select | ENSP00000358081.4:p.Gln33= | |
ENST00000369085.7:c.98_106delinsAGACCGGCT | ENSP00000358081.3:p.Gln33= | |
NM_004281.3:c.98_106delinsAGACCGGCT , LRG_742t1:c.98_106delinsAGACCGGCT | NP_004272.2:p.Gln33= | |
XM_005270287.1:c.98_106delinsAGACCGGCT | XP_005270344.1:p.Gln33= | |
XM_005270287.2:c.98_106delinsAGACCGGCT | XP_005270344.1:p.Gln33= | |
NM_004281.4:c.98_106delinsAGACCGGCT MANE Select | NP_004272.2:p.Gln33= |