HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34793540G>T , CM000677.2:g.34793540G>T | GRCh38 |
NC_000015.9:g.35085741G>T , CM000677.1:g.35085741G>T | GRCh37 |
NC_000015.8:g.32873033G>T | NCBI36 |
NG_007553.1:g.7187C>A , LRG_388:g.7187C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000560563.2:n.265C>A (ACTC1) | ||
ENST00000290378.6:c.159C>A (ACTC1) MANE Select | ENSP00000290378.4:p.Asp53Glu | |
ENST00000647798.1:n.306C>A (ACTC1) | ||
ENST00000648556.1:n.316C>A (ACTC1) | ||
ENST00000650163.1:n.239C>A (ACTC1) | ||
ENST00000290378.4:c.159C>A (ACTC1) | ENSP00000290378.4:p.Asp53Glu | |
NM_005159.4:c.159C>A , LRG_388t1:c.159C>A (ACTC1) | NP_005150.1:p.Asp53Glu | |
NR_120329.1:n.299+16109G>T (GJD2-DT) | ||
NM_005159.5:c.159C>A (ACTC1) MANE Select | NP_005150.1:p.Asp53Glu |