Linked Data
dbSNP Id:
rs1971901515
gnomAD v3:
19-45353495-G-GTTCCCCACCCA
gnomAD v4:
19-45353495-G-GTTCCCCACCCA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45353495_45353496insTTCCCCACCCA , CM000681.2:g.45353495_45353496insTTCCCCACCCA | GRCh38 |
| NC_000019.9:g.45856753_45856754insTTCCCCACCCA , CM000681.1:g.45856753_45856754insTTCCCCACCCA | GRCh37 |
| NC_000019.8:g.50548593_50548594insTTCCCCACCCA | NCBI36 |
| NG_007067.2:g.22092_22093insTGGGTGGGGAA , LRG_461:g.22092_22093insTGGGTGGGGAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000391944.8:c.1666-162_1666-161insTGGGTGGGGAA | ENSP00000375808.4:n.1666-162_1666-161insTGGGTGGGGAA | |
| ENST00000682414.1:c.1666-162_1666-161insTGGGTGGGGAA | ENSP00000507019.1:n.1666-162_1666-161insTGGGTGGGGAA | |
| ENST00000682508.1:n.1695-162_1695-161insTGGGTGGGGAA | ||
| ENST00000684218.1:c.*924-162_*924-161insTGGGTGGGGAA | ENSP00000507804.1:n.*924-162_*924-161insTGGGTGGGGAA | |
| ENST00000684264.1:n.1222-162_1222-161insTGGGTGGGGAA | ||
| ENST00000684407.1:c.1543-162_1543-161insTGGGTGGGGAA | ENSP00000507775.1:n.1543-162_1543-161insTGGGTGGGGAA | |
| ENST00000684458.1:c.*152-162_*152-161insTGGGTGGGGAA | ENSP00000508260.1:n.*152-162_*152-161insTGGGTGGGGAA | |
| ENST00000684468.1:n.1378-162_1378-161insTGGGTGGGGAA | ||
| ENST00000391945.10:c.1666-162_1666-161insTGGGTGGGGAA MANE Select | ENSP00000375809.4:n.1666-162_1666-161insTGGGTGGGGAA | |
| ENST00000587376.6:c.725-162_725-161insTGGGTGGGGAA | ||
| ENST00000646507.1:n.1763-162_1763-161insTGGGTGGGGAA | ||
| ENST00000391941.6:c.1594-162_1594-161insTGGGTGGGGAA | ENSP00000375805.2:n.1594-162_1594-161insTGGGTGGGGAA | |
| ENST00000391942.6:n.837-162_837-161insTGGGTGGGGAA | ||
| ENST00000391944.7:c.1432-162_1432-161insTGGGTGGGGAA | ENSP00000375808.3:n.1432-162_1432-161insTGGGTGGGGAA | |
| ENST00000391945.8:c.1666-162_1666-161insTGGGTGGGGAA | ENSP00000375809.3:n.1666-162_1666-161insTGGGTGGGGAA | |
| ENST00000587376.5:c.725-162_725-161insTGGGTGGGGAA | ||
| ENST00000588652.5:n.1754-162_1754-161insTGGGTGGGGAA | ||
| NM_000400.3:c.1666-162_1666-161insTGGGTGGGGAA , LRG_461t1:c.1666-162_1666-161insTGGGTGGGGAA | NP_000391.1:n.1666-162_1666-161insTGGGTGGGGAA | |
| XM_011526611.1:c.1588-162_1588-161insTGGGTGGGGAA | XP_011524913.1:n.1588-162_1588-161insTGGGTGGGGAA | |
| XR_935763.1:n.1649-162_1649-161insTGGGTGGGGAA | ||
| XM_011526611.2:c.1588-162_1588-161insTGGGTGGGGAA | XP_011524913.1:n.1588-162_1588-161insTGGGTGGGGAA | |
| XM_017026467.1:c.1543-162_1543-161insTGGGTGGGGAA | XP_016881956.1:n.1543-162_1543-161insTGGGTGGGGAA | |
| XR_001753633.2:n.1713-162_1713-161insTGGGTGGGGAA | ||
| XR_001753634.2:n.1649-162_1649-161insTGGGTGGGGAA | ||
| NM_000400.4:c.1666-162_1666-161insTGGGTGGGGAA MANE Select | NP_000391.1:n.1666-162_1666-161insTGGGTGGGGAA |