Canonical Allele Identifier: CA377513618

Gene: ACTA2 STAMBPL1

Linked Data

• MyVariant Identifiers: chr10:g.90708578A>G (hg19) ; chr10:g.88948821A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88948821A>G , CM000672.2:g.88948821A>G	GRCh38
NC_000010.10:g.90708578A>G , CM000672.1:g.90708578A>G	GRCh37
NC_000010.9:g.90698558A>G	NCBI36
NG_011541.1:g.47570T>C , LRG_781:g.47570T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415557.2:c.110T>C (ACTA2)	ENSP00000396730.2:p.Val37Ala
ENST00000458159.6:c.110T>C (ACTA2)	ENSP00000398239.2:p.Val37Ala
ENST00000480297.6:n.176T>C (ACTA2)
ENST00000482085.2:n.176T>C (ACTA2)
ENST00000224784.10:c.110T>C (ACTA2) MANE Select	ENSP00000224784.6:p.Val37Ala
ENST00000371927.7:c.1255-24361A>G (STAMBPL1)	ENSP00000360995.3:n.1255-24361A>G
ENST00000415557.1:c.110T>C (ACTA2)	ENSP00000396730.1:p.Val37Ala
ENST00000458159.5:c.110T>C (ACTA2)	ENSP00000398239.1:p.Val37Ala
ENST00000458208.5:c.110T>C (ACTA2)	ENSP00000402373.1:p.Val37Ala
ENST00000480297.5:n.150T>C (ACTA2)
ENST00000482085.1:n.176T>C (ACTA2)
ENST00000488967.5:n.176T>C (ACTA2)
NM_001141945.1:c.110T>C , LRG_781t2:c.110T>C (ACTA2)	NP_001135417.1:p.Val37Ala
NM_001613.2:c.110T>C , LRG_781t1:c.110T>C (ACTA2)	NP_001604.1:p.Val37Ala
XM_011540016.1:c.110T>C (ACTA2)	XP_011538318.1:p.Val37Ala
NM_001141945.2:c.110T>C (ACTA2)	NP_001135417.1:p.Val37Ala
NM_001320855.1:c.110T>C (ACTA2)	NP_001307784.1:p.Val37Ala
NM_001613.3:c.110T>C (ACTA2)	NP_001604.1:p.Val37Ala
NM_001613.4:c.110T>C (ACTA2) MANE Select	NP_001604.1:p.Val37Ala