HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104034200_104034204delinsCAGAT , CM000672.2:g.104034200_104034204delinsCAGAT | GRCh38 |
NC_000010.10:g.105793958_105793962delinsCAGAT , CM000672.1:g.105793958_105793962delinsCAGAT | GRCh37 |
NC_000010.9:g.105783948_105783952delinsCAGAT | NCBI36 |
NG_007069.1:g.56677_56681delinsATCTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.3651_3655delinsATCTG | ENSP00000358748.3:p.Ser1217= | |
ENST00000648076.2:c.3897_3901delinsATCTG MANE Select | ENSP00000497653.1:p.Ser1299= | |
ENST00000353479.9:c.3897_3901delinsATCTG | ENSP00000340937.5:p.Ser1299= | |
ENST00000369733.7:c.3651_3655delinsATCTG | ENSP00000358748.3:p.Ser1217= | |
NM_000494.3:c.3897_3901delinsATCTG | NP_000485.3:p.Ser1299= | |
NM_000494.4:c.3897_3901delinsATCTG MANE Select | NP_000485.3:p.Ser1299= |