Canonical Allele Identifier: CA2788919367

Gene: ACTA2 STAMBPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88946920T>A , CM000672.2:g.88946920T>A	GRCh38
NC_000010.10:g.90706677T>A , CM000672.1:g.90706677T>A	GRCh37
NC_000010.9:g.90696657T>A	NCBI36
NG_011541.1:g.49471A>T , LRG_781:g.49471A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415557.2:c.258+338A>T (ACTA2)	ENSP00000396730.2:n.258+338A>T
ENST00000458159.6:c.258+338A>T (ACTA2)	ENSP00000398239.2:n.258+338A>T
ENST00000480297.6:n.324+338A>T (ACTA2)
ENST00000482085.2:n.1739+338A>T (ACTA2)
ENST00000224784.10:c.258+338A>T (ACTA2) MANE Select	ENSP00000224784.6:n.258+338A>T
ENST00000371927.7:c.1254+24484T>A (STAMBPL1)	ENSP00000360995.3:n.1254+24484T>A
ENST00000415557.1:c.258+338A>T (ACTA2)	ENSP00000396730.1:n.258+338A>T
ENST00000458159.5:c.258+338A>T (ACTA2)	ENSP00000398239.1:n.258+338A>T
ENST00000458208.5:c.258+338A>T (ACTA2)	ENSP00000402373.1:n.258+338A>T
ENST00000480297.5:n.298+338A>T (ACTA2)
ENST00000488967.5:n.662A>T (ACTA2)
NM_001141945.1:c.258+338A>T , LRG_781t2:c.258+338A>T (ACTA2)	NP_001135417.1:n.258+338A>T
NM_001613.2:c.258+338A>T , LRG_781t1:c.258+338A>T (ACTA2)	NP_001604.1:n.258+338A>T
XM_011540016.1:c.258+338A>T (ACTA2)	XP_011538318.1:n.258+338A>T
NM_001141945.2:c.258+338A>T (ACTA2)	NP_001135417.1:n.258+338A>T
NM_001320855.1:c.258+338A>T (ACTA2)	NP_001307784.1:n.258+338A>T
NM_001613.3:c.258+338A>T (ACTA2)	NP_001604.1:n.258+338A>T
NM_001613.4:c.258+338A>T (ACTA2) MANE Select	NP_001604.1:n.258+338A>T