HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202927_32202929delinsCAG , CM000668.2:g.32202927_32202929delinsCAG | GRCh38 |
NC_000006.11:g.32170704_32170706delinsCAG , CM000668.1:g.32170704_32170706delinsCAG | GRCh37 |
NC_000006.10:g.32278682_32278684delinsCAG | NCBI36 |
NG_028190.1:g.26139_26141delinsCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-330_3232-328delinsCTG MANE Select | ENSP00000364163.3:n.3232-330_3232-328delinsCTG | |
ENST00000474612.1:n.988_990delinsCTG | ||
NM_004557.3:c.3232-330_3232-328delinsCTG | NP_004548.3:n.3232-330_3232-328delinsCTG | |
NR_134949.1:n.3472+841_3472+843delinsCTG | ||
NR_134950.1:n.3370+841_3370+843delinsCTG | ||
NM_004557.4:c.3232-330_3232-328delinsCTG MANE Select | NP_004548.3:n.3232-330_3232-328delinsCTG | |
NR_134949.2:n.3472+841_3472+843delinsCTG | ||
NR_134950.2:n.3370+841_3370+843delinsCTG |