Canonical Allele Identifier: CA1926598106
Gene: ACTA2 HGNC NCBI
STAMBPL1 HGNC NCBI
ACTA2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1845719144

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88935502_88935503insA , CM000672.2:g.88935502_88935503insA GRCh38
NC_000010.10:g.90695259_90695260insA , CM000672.1:g.90695259_90695260insA GRCh37
NC_000010.9:g.90685239_90685240insA NCBI36
NG_011541.1:g.60888_60889insT , LRG_781:g.60888_60889insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000415557.2:c.991-137_991-136insT (ACTA2) ENSP00000396730.2:n.991-137_991-136insT
ENST00000458159.6:c.991-137_991-136insT (ACTA2) ENSP00000398239.2:n.991-137_991-136insT
ENST00000480297.6:n.2587-137_2587-136insT (ACTA2)
ENST00000224784.10:c.991-137_991-136insT (ACTA2) MANE Select ENSP00000224784.6:n.991-137_991-136insT
ENST00000371927.7:c.1254+13066_1254+13067insA (STAMBPL1) ENSP00000360995.3:n.1254+13066_1254+13067insA
ENST00000458208.5:c.991-137_991-136insT (ACTA2) ENSP00000402373.1:n.991-137_991-136insT
NM_001141945.1:c.991-137_991-136insT , LRG_781t2:c.991-137_991-136insT (ACTA2) NP_001135417.1:n.991-137_991-136insT
NM_001613.2:c.991-137_991-136insT , LRG_781t1:c.991-137_991-136insT (ACTA2) NP_001604.1:n.991-137_991-136insT
NR_125373.1:n.1127_1128insA (ACTA2-AS1)
XM_011540016.1:c.991-137_991-136insT (ACTA2) XP_011538318.1:n.991-137_991-136insT
NM_001141945.2:c.991-137_991-136insT (ACTA2) NP_001135417.1:n.991-137_991-136insT
NM_001320855.1:c.991-137_991-136insT (ACTA2) NP_001307784.1:n.991-137_991-136insT
NM_001613.3:c.991-137_991-136insT (ACTA2) NP_001604.1:n.991-137_991-136insT
NM_001613.4:c.991-137_991-136insT (ACTA2) MANE Select NP_001604.1:n.991-137_991-136insT