Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160030758T>A , CM000663.2:g.160030758T>A | GRCh38 |
| NC_000001.10:g.160000548T>A , CM000663.1:g.160000548T>A | GRCh37 |
| NC_000001.9:g.158267172T>A | NCBI36 |
| NG_012238.1:g.6236A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368090.5:c.982A>T (PIGM) MANE Select | ENSP00000357069.2:p.Asn328Tyr | |
| ENST00000509700.2:c.671+11076A>T (KCNJ10) | ||
| ENST00000637644.1:c.487+11288A>T (KCNJ10) | ENSP00000490282.1:n.487+11288A>T | |
| ENST00000639408.1:c.587+9744A>T (KCNJ10) | ENSP00000491635.1:n.587+9744A>T | |
| ENST00000640914.1:c.224+9744A>T (KCNJ10) | ||
| ENST00000368090.3:c.982A>T (PIGM) | ENSP00000357069.2:p.Asn328Tyr | |
| NM_145167.2:c.982A>T (PIGM) | NP_660150.1:p.Asn328Tyr | |
| NM_145167.3:c.982A>T (PIGM) MANE Select | NP_660150.1:p.Asn328Tyr |