Linked Data
dbSNP Id:
rs1555416695
gnomAD v2:
15-78887190-TAATC-T
gnomAD v3:
15-78594848-TAATC-T
gnomAD v4:
15-78594848-TAATC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.78594853_78594856del , CM000677.2:g.78594853_78594856del | GRCh38 |
| NC_000015.9:g.78887195_78887198del , CM000677.1:g.78887195_78887198del | GRCh37 |
| NC_000015.8:g.76674250_76674253del | NCBI36 |
| NG_016143.1:g.31444_31447del | |
| NG_023328.1:g.34334_34337del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299565.9:c.*1600_*1603del (CHRNA5) MANE Select | ENSP00000299565.5:n.*1600_*1603del | |
| ENST00000348639.7:c.1390-1661_1390-1658del (CHRNA3) | ENSP00000267951.4:n.1390-1661_1390-1658del | |
| ENST00000559002.5:n.194-1661_194-1658del (CHRNA3) | ||
| ENST00000559658.5:c.*65-841_*65-838del (CHRNA3) | ENSP00000452896.1:n.*65-841_*65-838del | |
| NM_000745.3:c.*1600_*1603del (CHRNA5) | NP_000736.2:n.*1600_*1603del | |
| NM_001166694.1:c.1390-1661_1390-1658del (CHRNA3) | NP_001160166.1:n.1390-1661_1390-1658del | |
| NM_001307945.1:c.*1737_*1740del (CHRNA5) | NP_001294874.1:n.*1737_*1740del | |
| NR_046313.1:n.2084-841_2084-838del (CHRNA3) | ||
| NM_001166694.2:c.1390-1661_1390-1658del (CHRNA3) | NP_001160166.1:n.1390-1661_1390-1658del | |
| NM_001307945.2:c.*1737_*1740del (CHRNA5) | NP_001294874.1:n.*1737_*1740del | |
| NR_046313.2:n.1785-841_1785-838del (CHRNA3) | ||
| NM_000745.4:c.*1600_*1603del (CHRNA5) MANE Select | NP_000736.2:n.*1600_*1603del | |
| NM_001395171.1:c.*1737_*1740del (CHRNA5) | NP_001382100.1:n.*1737_*1740del | |
| NM_001395172.1:c.*1600_*1603del (CHRNA5) | NP_001382101.1:n.*1600_*1603del | |
| NM_001395173.1:c.*1737_*1740del (CHRNA5) | NP_001382102.1:n.*1737_*1740del | |
| NM_001395174.1:c.*1737_*1740del (CHRNA5) | NP_001382103.1:n.*1737_*1740del | |
| NM_001395175.1:c.*1737_*1740del (CHRNA5) | NP_001382104.1:n.*1737_*1740del |