HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175977_70175983delinsGCTCTTA , CM000679.2:g.70175977_70175983delinsGCTCTTA | GRCh38 |
NC_000017.10:g.68172118_68172124delinsGCTCTTA , CM000679.1:g.68172118_68172124delinsGCTCTTA | GRCh37 |
NC_000017.9:g.65683713_65683719delinsGCTCTTA | NCBI36 |
NG_008798.1:g.11443_11449delinsGCTCTTA , LRG_328:g.11443_11449delinsGCTCTTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000243457.4:c.938_944delinsGCTCTTA MANE Select | ENSP00000243457.2:p.Ser313= | |
ENST00000243457.3:c.938_944delinsGCTCTTA | ENSP00000243457.2:p.Ser313= | |
ENST00000535240.1:c.938_944delinsGCTCTTA | ENSP00000441848.1:p.Ser313= | |
NM_000891.2:c.938_944delinsGCTCTTA , LRG_328t1:c.938_944delinsGCTCTTA | NP_000882.1:p.Ser313= | |
XM_011524779.1:c.938_944delinsGCTCTTA | XP_011523081.1:p.Ser313= | |
NM_000891.3:c.938_944delinsGCTCTTA MANE Select | NP_000882.1:p.Ser313= |