Canonical Allele Identifier: CA470728612

Gene: ACTA2 STAMBPL1 ACTA2-AS1

Linked Data

• MyVariant Identifiers: chr10:g.90694833A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88935076A>T , CM000672.2:g.88935076A>T	GRCh38
NC_000010.10:g.90694833A>T , CM000672.1:g.90694833A>T	GRCh37
NC_000010.9:g.90684813A>T	NCBI36
NG_011541.1:g.61315T>A , LRG_781:g.61315T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000458159.6:c.*147T>A (ACTA2)	ENSP00000398239.2:n.*147T>A
ENST00000224784.10:c.*147T>A (ACTA2) MANE Select	ENSP00000224784.6:n.*147T>A
ENST00000371927.7:c.1254+12640A>T (STAMBPL1)	ENSP00000360995.3:n.1254+12640A>T
ENST00000458208.5:c.*147T>A (ACTA2)	ENSP00000402373.1:n.*147T>A
NM_001141945.1:c.*147T>A , LRG_781t2:c.*147T>A (ACTA2)	NP_001135417.1:n.*147T>A
NM_001613.2:c.*147T>A , LRG_781t1:c.*147T>A (ACTA2)	NP_001604.1:n.*147T>A
NR_125373.1:n.701A>T (ACTA2-AS1)
XM_011540016.1:c.*147T>A (ACTA2)	XP_011538318.1:n.*147T>A
NM_001141945.2:c.*147T>A (ACTA2)	NP_001135417.1:n.*147T>A
NM_001320855.1:c.*147T>A (ACTA2)	NP_001307784.1:n.*147T>A
NM_001613.3:c.*147T>A (ACTA2)	NP_001604.1:n.*147T>A
NM_001613.4:c.*147T>A (ACTA2) MANE Select	NP_001604.1:n.*147T>A