Canonical Allele Identifier: CA377513692
Gene: ACTA2 HGNC NCBI
STAMBPL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 927995
dbSNP Id: rs1438979811

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88948855C>G , CM000672.2:g.88948855C>G GRCh38
NC_000010.10:g.90708612C>G , CM000672.1:g.90708612C>G GRCh37
NC_000010.9:g.90698592C>G NCBI36
NG_011541.1:g.47536G>C , LRG_781:g.47536G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000415557.2:c.76G>C (ACTA2) ENSP00000396730.2:p.Asp26His
ENST00000458159.6:c.76G>C (ACTA2) ENSP00000398239.2:p.Asp26His
ENST00000480297.6:n.142G>C (ACTA2)
ENST00000482085.2:n.142G>C (ACTA2)
ENST00000224784.10:c.76G>C (ACTA2) MANE Select ENSP00000224784.6:p.Asp26His
ENST00000371927.7:c.1255-24327C>G (STAMBPL1) ENSP00000360995.3:n.1255-24327C>G
ENST00000415557.1:c.76G>C (ACTA2) ENSP00000396730.1:p.Asp26His
ENST00000458159.5:c.76G>C (ACTA2) ENSP00000398239.1:p.Asp26His
ENST00000458208.5:c.76G>C (ACTA2) ENSP00000402373.1:p.Asp26His
ENST00000480297.5:n.116G>C (ACTA2)
ENST00000482085.1:n.142G>C (ACTA2)
ENST00000488967.5:n.142G>C (ACTA2)
NM_001141945.1:c.76G>C , LRG_781t2:c.76G>C (ACTA2) NP_001135417.1:p.Asp26His
NM_001613.2:c.76G>C , LRG_781t1:c.76G>C (ACTA2) NP_001604.1:p.Asp26His
XM_011540016.1:c.76G>C (ACTA2) XP_011538318.1:p.Asp26His
NM_001141945.2:c.76G>C (ACTA2) NP_001135417.1:p.Asp26His
NM_001320855.1:c.76G>C (ACTA2) NP_001307784.1:p.Asp26His
NM_001613.3:c.76G>C (ACTA2) NP_001604.1:p.Asp26His
NM_001613.4:c.76G>C (ACTA2) MANE Select NP_001604.1:p.Asp26His