HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780366_94780367delinsCT , CM000672.2:g.94780366_94780367delinsCT | GRCh38 |
NC_000010.10:g.96540123_96540124delinsCT , CM000672.1:g.96540123_96540124delinsCT | GRCh37 |
NC_000010.9:g.96530113_96530114delinsCT | NCBI36 |
NG_008384.2:g.22661_22662delinsCT | |
NG_008384.3:g.22686_22687delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.482-133_482-132delinsCT MANE Select | ENSP00000360372.3:n.482-133_482-132delins... | |
ENST00000645461.1:n.1535-133_1535-132delinsCT | ||
ENST00000371321.7:c.482-133_482-132delinsCT | ENSP00000360372.3:n.482-133_482-132delins... | |
ENST00000464755.1:c.1245-133_1245-132delinsCT | ENSP00000483243.1:n.1245-133_1245-132deli... | |
NM_000769.2:c.482-133_482-132delinsCT | NP_000760.1:n.482-133_482-132delinsCT | |
NM_000769.4:c.482-133_482-132delinsCT MANE Select | NP_000760.1:n.482-133_482-132delinsCT |