HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19116923_19116924delinsCT , CM000669.2:g.19116923_19116924delinsCT | GRCh38 |
NC_000007.13:g.19156546_19156547delinsCT , CM000669.1:g.19156546_19156547delinsCT | GRCh37 |
NC_000007.12:g.19123071_19123072delinsCT | NCBI36 |
NG_008114.1:g.5749_5750delinsAG | |
NG_008114.2:g.5749_5750delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000242261.6:c.398_399delinsAG MANE Select | ENSP00000242261.5:p.Lys133= | |
ENST00000242261.5:c.398_399delinsAG | ENSP00000242261.5:p.Lys133= | |
ENST00000354571.5:c.195_196delinsAG | ||
ENST00000443687.5:c.1_2delinsAG | ||
NM_000474.3:c.398_399delinsAG | NP_000465.1:p.Lys133= | |
XM_011515496.1:c.398_399delinsAG | XP_011513798.1:p.Lys133= | |
NR_149001.1:n.749_750delinsAG | ||
NM_000474.4:c.398_399delinsAG MANE Select | NP_000465.1:p.Lys133= | |
NR_149001.2:n.713_714delinsAG |