HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149981464_149981467delinsAAGT , CM000667.2:g.149981464_149981467delinsAAGT | GRCh38 |
NC_000005.9:g.149361027_149361030delinsAAGT , CM000667.1:g.149361027_149361030delinsAAGT | GRCh37 |
NC_000005.8:g.149341220_149341223delinsAAGT | NCBI36 |
NG_007147.2:g.22582_22585delinsAAGT , LRG_684:g.22582_22585delinsAAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.1871_1874delinsAAGT MANE Select | ENSP00000286298.4:p.Lys624= | |
ENST00000286298.4:c.1871_1874delinsAAGT | ENSP00000286298.4:p.Lys624= | |
ENST00000503336.1:c.372+3113_372+3116delinsAAGT | ENSP00000426053.1:n.372+3113_372+3116delinsAAGT | |
NM_000112.3:c.1871_1874delinsAAGT , LRG_684t1:c.1871_1874delinsAAGT | NP_000103.2:p.Lys624= | |
XM_017009191.2:c.1871_1874delinsAAGT | XP_016864680.1:p.Lys624= | |
NM_000112.4:c.1871_1874delinsAAGT MANE Select | NP_000103.2:p.Lys624= |