Linked Data
dbSNP Id:
rs4075583
gnomAD v2:
15-63340227-G-A
gnomAD v3:
15-63048028-G-A
gnomAD v4:
15-63048028-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.63048028G>A , CM000677.2:g.63048028G>A | GRCh38 |
| NC_000015.9:g.63340227G>A , CM000677.1:g.63340227G>A | GRCh37 |
| NC_000015.8:g.61127280G>A | NCBI36 |
| NG_007557.1:g.10390G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000559831.6:c.240+3876G>A (TPM1) | ENSP00000452977.2:n.240+3876G>A | |
| ENST00000560131.2:n.319+3876G>A (TPM1) | ||
| ENST00000561395.6:c.240+3876G>A (TPM1) | ENSP00000453092.2:n.240+3876G>A | |
| ENST00000357980.9:c.366+3876G>A (TPM1) | ENSP00000350667.4:n.366+3876G>A | |
| ENST00000403994.9:c.240+3876G>A (TPM1) MANE Select | ENSP00000385107.4:n.240+3876G>A | |
| ENST00000559397.6:c.240+4197G>A (TPM1) | ENSP00000452879.1:n.240+4197G>A | |
| ENST00000560970.6:c.240+3876G>A (TPM1) | ENSP00000453062.2:n.240+3876G>A | |
| ENST00000561266.6:c.240+4197G>A (TPM1) | ENSP00000453955.2:n.240+4197G>A | |
| ENST00000644204.1:n.186+3876G>A (TPM1) | ||
| ENST00000651344.1:n.422+3876G>A (TPM1) | ||
| ENST00000267996.11:c.240+4197G>A (TPM1) | ENSP00000267996.7:n.240+4197G>A | |
| ENST00000288398.10:c.240+3876G>A (TPM1) | ENSP00000288398.6:n.240+3876G>A | |
| ENST00000357980.8:c.366+3876G>A (TPM1) | ENSP00000350667.4:n.366+3876G>A | |
| ENST00000358278.7:c.240+3876G>A (TPM1) | ENSP00000351022.3:n.240+3876G>A | |
| ENST00000403994.7:c.240+3876G>A (TPM1) | ENSP00000385107.3:n.240+3876G>A | |
| ENST00000558314.5:n.640+3876G>A (TPM1) | ||
| ENST00000558347.5:c.240+3876G>A (TPM1) | ENSP00000452887.1:n.240+3876G>A | |
| ENST00000559397.5:c.240+4197G>A (TPM1) | ENSP00000452879.1:n.240+4197G>A | |
| ENST00000559556.5:c.240+3876G>A (TPM1) | ENSP00000453941.1:n.240+3876G>A | |
| ENST00000559831.5:c.12+3876G>A (TPM1) | ENSP00000452977.1:n.12+3876G>A | |
| ENST00000560445.1:c.186+3930G>A (TPM1) | ENSP00000452999.1:n.186+3930G>A | |
| ENST00000560970.5:c.182+3876G>A (TPM1) | ||
| ENST00000560975.5:n.1148+4197G>A (TPM1) | ||
| ENST00000561266.5:c.56+4197G>A (TPM1) | ||
| ENST00000561425.5:c.*354+4197G>A (TPM1) | ENSP00000453324.1:n.*354+4197G>A | |
| NM_000366.5:c.240+3876G>A (TPM1) | NP_000357.3:n.240+3876G>A | |
| NM_001018004.1:c.240+3876G>A (TPM1) | NP_001018004.1:n.240+3876G>A | |
| NM_001018005.1:c.240+3876G>A (TPM1) | NP_001018005.1:n.240+3876G>A | |
| NM_001018006.1:c.240+3876G>A (TPM1) | NP_001018006.1:n.240+3876G>A | |
| NM_001018007.1:c.240+4197G>A (TPM1) | NP_001018007.1:n.240+4197G>A | |
| NM_001018020.1:c.240+4197G>A (TPM1) | NP_001018020.1:n.240+4197G>A | |
| NM_001301244.1:c.240+4197G>A (TPM1) | NP_001288173.1:n.240+4197G>A | |
| XM_005254637.1:c.366+3876G>A (TPM1) | XP_005254694.1:n.366+3876G>A | |
| XM_005254638.2:c.240+3876G>A (TPM1) | XP_005254695.1:n.240+3876G>A | |
| XM_005254639.2:c.240+3876G>A (TPM1) | XP_005254696.1:n.240+3876G>A | |
| XM_005254640.2:c.240+4197G>A (TPM1) | XP_005254697.1:n.240+4197G>A | |
| XM_005254641.2:c.240+4197G>A (TPM1) | XP_005254698.1:n.240+4197G>A | |
| XM_005254645.1:c.240+3876G>A (TPM1) | XP_005254702.1:n.240+3876G>A | |
| XM_006720667.2:c.240+3876G>A (TPM1) | XP_006720730.1:n.240+3876G>A | |
| XM_006720669.2:c.-139+3876G>A (TPM1) | XP_006720732.1:n.-139+3876G>A | |
| NM_001365776.1:c.240+3876G>A (TPM1) | NP_001352705.1:n.240+3876G>A | |
| NM_001365777.1:c.240+3876G>A (TPM1) | NP_001352706.1:n.240+3876G>A | |
| NM_001365778.1:c.366+3876G>A (TPM1) | NP_001352707.1:n.366+3876G>A | |
| NM_001365779.1:c.240+3876G>A (TPM1) | NP_001352708.1:n.240+3876G>A | |
| NR_147233.2:n.1215C>T (TPM1-AS) | ||
| XM_005254639.4:c.240+3876G>A (TPM1) | XP_005254696.3:n.240+3876G>A | |
| XM_006720667.4:c.240+3876G>A (TPM1) | XP_006720730.3:n.240+3876G>A | |
| XM_017022534.2:c.240+3876G>A (TPM1) | XP_016878023.2:n.240+3876G>A | |
| XM_017022535.2:c.240+4197G>A (TPM1) | XP_016878024.1:n.240+4197G>A | |
| XM_017022536.2:c.240+3876G>A (TPM1) | XP_016878025.2:n.240+3876G>A | |
| XM_017022537.2:c.240+4197G>A (TPM1) | XP_016878026.1:n.240+4197G>A | |
| XM_017022538.2:c.240+3876G>A (TPM1) | XP_016878027.2:n.240+3876G>A | |
| XM_017022539.2:c.240+3876G>A (TPM1) | XP_016878028.2:n.240+3876G>A | |
| XM_024450040.1:c.-139+3876G>A (TPM1) | XP_024305808.1:n.-139+3876G>A | |
| NM_000366.6:c.240+3876G>A (TPM1) | NP_000357.3:n.240+3876G>A | |
| NM_001018004.2:c.240+3876G>A (TPM1) | NP_001018004.1:n.240+3876G>A | |
| NM_001018005.2:c.240+3876G>A (TPM1) MANE Select | NP_001018005.1:n.240+3876G>A | |
| NM_001018006.2:c.240+3876G>A (TPM1) | NP_001018006.1:n.240+3876G>A | |
| NM_001018007.2:c.240+4197G>A (TPM1) | NP_001018007.1:n.240+4197G>A | |
| NM_001018020.2:c.240+4197G>A (TPM1) | NP_001018020.1:n.240+4197G>A | |
| NM_001301244.2:c.240+4197G>A (TPM1) | NP_001288173.1:n.240+4197G>A |