HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48459690dup , CM000675.2:g.48459690dup | GRCh38 |
NC_000013.10:g.49033826dup , CM000675.1:g.49033826dup | GRCh37 |
NC_000013.9:g.47931827dup | NCBI36 |
NG_009009.1:g.160944dup , LRG_517:g.160944dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000267163.6:c.1963dup MANE Select | ENSP00000267163.4:p.Tyr655LeufsTer13 | |
ENST00000643064.1:c.194+78247dup | ||
ENST00000650461.1:c.1963dup | ENSP00000497193.1:p.Tyr655LeufsTer13 | |
ENST00000267163.4:c.1963dup | ENSP00000267163.4:p.Tyr655LeufsTer13 | |
NM_000321.2:c.1963dup , LRG_517t1:c.1963dup | NP_000312.2:p.Tyr655LeufsTer13 | |
XM_011535171.1:c.1702dup | XP_011533473.1:p.Tyr568LeufsTer13 | |
XM_011535171.2:c.1702dup | XP_011533473.1:p.Tyr568LeufsTer13 | |
NM_000321.3:c.1963dup MANE Select | NP_000312.2:p.Tyr655LeufsTer13 |