HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104034709_104034715del , CM000672.2:g.104034709_104034715del | GRCh38 |
NC_000010.10:g.105794467_105794473del , CM000672.1:g.105794467_105794473del | GRCh37 |
NC_000010.9:g.105784457_105784463del | NCBI36 |
NG_007069.1:g.56167_56173del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.3427_3433del | ENSP00000358748.3:p.Pro1143GlyfsTer24 | |
ENST00000648076.2:c.3673_3679del MANE Select | ENSP00000497653.1:p.Pro1225GlyfsTer24 | |
ENST00000353479.9:c.3673_3679del | ENSP00000340937.5:p.Pro1225GlyfsTer24 | |
ENST00000369733.7:c.3427_3433del | ENSP00000358748.3:p.Pro1143GlyfsTer24 | |
NM_000494.3:c.3673_3679del | NP_000485.3:p.Pro1225GlyfsTer24 | |
NM_000494.4:c.3673_3679del MANE Select | NP_000485.3:p.Pro1225GlyfsTer24 |