Canonical Allele Identifier: CA377510602

Gene: ACTA2 STAMBPL1 ACTA2-AS1

Linked Data

• ClinVar Variation Id: 572632
• ClinVar RCV Id: RCV000694059
• dbSNP Id: rs1564641192
• MyVariant Identifiers: chr10:g.90695108C>G (hg19) ; chr10:g.88935351C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88935351C>G , CM000672.2:g.88935351C>G	GRCh38
NC_000010.10:g.90695108C>G , CM000672.1:g.90695108C>G	GRCh37
NC_000010.9:g.90685088C>G	NCBI36
NG_011541.1:g.61040G>C , LRG_781:g.61040G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415557.2:c.1006G>C (ACTA2)	ENSP00000396730.2:p.Glu336Gln
ENST00000458159.6:c.1006G>C (ACTA2)	ENSP00000398239.2:p.Glu336Gln
ENST00000480297.6:n.2602G>C (ACTA2)
ENST00000224784.10:c.1006G>C (ACTA2) MANE Select	ENSP00000224784.6:p.Glu336Gln
ENST00000371927.7:c.1254+12915C>G (STAMBPL1)	ENSP00000360995.3:n.1254+12915C>G
ENST00000458208.5:c.1006G>C (ACTA2)	ENSP00000402373.1:p.Glu336Gln
NM_001141945.1:c.1006G>C , LRG_781t2:c.1006G>C (ACTA2)	NP_001135417.1:p.Glu336Gln
NM_001613.2:c.1006G>C , LRG_781t1:c.1006G>C (ACTA2)	NP_001604.1:p.Glu336Gln
NR_125373.1:n.976C>G (ACTA2-AS1)
XM_011540016.1:c.1006G>C (ACTA2)	XP_011538318.1:p.Glu336Gln
NM_001141945.2:c.1006G>C (ACTA2)	NP_001135417.1:p.Glu336Gln
NM_001320855.1:c.1006G>C (ACTA2)	NP_001307784.1:p.Glu336Gln
NM_001613.3:c.1006G>C (ACTA2)	NP_001604.1:p.Glu336Gln
NM_001613.4:c.1006G>C (ACTA2) MANE Select	NP_001604.1:p.Glu336Gln