ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4900795_4900796delinsAA , CM000679.2:g.4900795_4900796delinsAA | GRCh38 |
| NC_000017.10:g.4804090_4804091delinsAA , CM000679.1:g.4804090_4804091delinsAA | GRCh37 |
| NC_000017.9:g.4744869_4744870delinsAA | NCBI36 |
| NG_008029.2:g.7280_7281delinsTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381365.4:c.*262_*263delinsAA (C17orf107) MANE Select | ENSP00000370770.3:n.*262_*263delinsAA | |
| ENST00000649488.2:c.914_915delinsTT (CHRNE) MANE Select | ENSP00000497829.1:p.Gly305Val | |
| ENST00000649830.1:c.-20_-19delinsTT (CHRNE) | ENSP00000496907.1:n.-20_-19delinsTT | |
| ENST00000293780.4:c.914_915delinsTT (CHRNE) | ENSP00000293780.4:p.Gly305Val | |
| ENST00000381365.3:c.*262_*263delinsAA (C17orf107) | ENSP00000370770.3:n.*262_*263delinsAA | |
| ENST00000521575.1:c.*629_*630delinsAA (C17orf107) | ENSP00000429241.1:n.*629_*630delinsAA | |
| ENST00000572438.1:n.600_601delinsTT (CHRNE) | ||
| NM_000080.3:c.914_915delinsTT (CHRNE) | NP_000071.1:p.Gly305Val | |
| NM_001145536.1:c.*262_*263delinsAA (C17orf107) | NP_001139008.1:n.*262_*263delinsAA | |
| XM_011523612.1:c.546+289_546+290delinsAA (C17orf107) | XP_011521914.1:n.546+289_546+290delinsAA | |
| XM_011523631.1:c.802+194_802+195delinsTT (CHRNE) | XP_011521933.1:n.802+194_802+195delinsTT | |
| NM_000080.4:c.914_915delinsTT (CHRNE) MANE Select | NP_000071.1:p.Gly305Val | |
| XM_017024115.1:c.878_879delinsTT (CHRNE) | XP_016879604.1:p.Gly293Val | |
| XR_001752421.1:n.1647+194_1647+195delinsTT (CHRNE) | ||
| NM_001145536.2:c.*262_*263delinsAA (C17orf107) MANE Select | NP_001139008.1:n.*262_*263delinsAA |