MyVariant.info:
GRCh37
chr6:g.132141012C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131819872C>A , CM000668.2:g.131819872C>A | GRCh38 |
| NC_000006.11:g.132141012C>A , CM000668.1:g.132141012C>A | GRCh37 |
| NC_000006.10:g.132182705C>A | NCBI36 |
| NG_008206.1:g.16857C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647893.1:c.240+11597C>A (ENPP1) MANE Select | ENSP00000498074.1:n.240+11597C>A | |
| ENST00000650507.1:c.154-6150C>A (ENPP1) | ENSP00000497375.1:n.154-6150C>A | |
| ENST00000360971.6:c.240+11597C>A (ENPP1) | ENSP00000354238.2:n.240+11597C>A | |
| ENST00000407837.2:n.220G>T (SELENOKP2) | ||
| ENST00000486853.1:n.260+11597C>A (ENPP1) | ||
| ENST00000513998.5:c.240+11597C>A (ENPP1) | ENSP00000422424.1:n.240+11597C>A | |
| NM_006208.2:c.240+11597C>A (ENPP1) | NP_006199.2:n.240+11597C>A | |
| NM_006208.3:c.240+11597C>A (ENPP1) MANE Select | NP_006199.2:n.240+11597C>A |