Canonical Allele Identifier: CA470728618

Gene: ACTA2 STAMBPL1 ACTA2-AS1

Linked Data

• MyVariant Identifiers: chr10:g.90694835C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88935078C>G , CM000672.2:g.88935078C>G	GRCh38
NC_000010.10:g.90694835C>G , CM000672.1:g.90694835C>G	GRCh37
NC_000010.9:g.90684815C>G	NCBI36
NG_011541.1:g.61313G>C , LRG_781:g.61313G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000458159.6:c.*145G>C (ACTA2)	ENSP00000398239.2:n.*145G>C
ENST00000224784.10:c.*145G>C (ACTA2) MANE Select	ENSP00000224784.6:n.*145G>C
ENST00000371927.7:c.1254+12642C>G (STAMBPL1)	ENSP00000360995.3:n.1254+12642C>G
ENST00000458208.5:c.*145G>C (ACTA2)	ENSP00000402373.1:n.*145G>C
NM_001141945.1:c.*145G>C , LRG_781t2:c.*145G>C (ACTA2)	NP_001135417.1:n.*145G>C
NM_001613.2:c.*145G>C , LRG_781t1:c.*145G>C (ACTA2)	NP_001604.1:n.*145G>C
NR_125373.1:n.703C>G (ACTA2-AS1)
XM_011540016.1:c.*145G>C (ACTA2)	XP_011538318.1:n.*145G>C
NM_001141945.2:c.*145G>C (ACTA2)	NP_001135417.1:n.*145G>C
NM_001320855.1:c.*145G>C (ACTA2)	NP_001307784.1:n.*145G>C
NM_001613.3:c.*145G>C (ACTA2)	NP_001604.1:n.*145G>C
NM_001613.4:c.*145G>C (ACTA2) MANE Select	NP_001604.1:n.*145G>C