HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48303921_48303922delinsCA , CM000675.2:g.48303921_48303922delinsCA | GRCh38 |
NC_000013.10:g.48878057_48878058delinsCA , CM000675.1:g.48878057_48878058delinsCA | GRCh37 |
NC_000013.9:g.47776058_47776059delinsCA | NCBI36 |
NG_009009.1:g.5175_5176delinsCA , LRG_517:g.5175_5176delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.9_10delinsCA MANE Select | ENSP00000267163.4:p.Pro3= | |
ENST00000646097.1:c.9_10delinsCA | ENSP00000496556.1:p.Pro3= | |
ENST00000650461.1:c.9_10delinsCA | ENSP00000497193.1:p.Pro3= | |
ENST00000267163.4:c.9_10delinsCA | ENSP00000267163.4:p.Pro3= | |
ENST00000467505.5:c.9_10delinsCA | ENSP00000434702.1:p.Pro3= | |
ENST00000525036.1:n.171_172delinsCA | ||
NM_000321.2:c.9_10delinsCA , LRG_517t1:c.9_10delinsCA | NP_000312.2:p.Pro3= | |
NM_000321.3:c.9_10delinsCA MANE Select | NP_000312.2:p.Pro3= |