Canonical Allele Identifier: CA1144880123

Gene: ACTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.229431700C= , CM000663.2:g.229431700C=	GRCh38
NC_000001.10:g.229567447C= , CM000663.1:g.229567447C=	GRCh37
NC_000001.9:g.227634070C=	NCBI36
NG_006672.1:g.7397G= , LRG_429:g.7397G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366683.4:c.990+21G=	ENSP00000355644.4:n.990+21G=
ENST00000684723.1:c.855+21G=	ENSP00000508084.1:n.855+21G=
ENST00000366683.3:c.621+21G=	ENSP00000355644.3:n.621+21G=
ENST00000366684.7:c.990+21G= MANE Select	ENSP00000355645.3:n.990+21G=
NM_001100.3:c.990+21G= , LRG_429t1:c.990+21G=	NP_001091.1:n.990+21G=
NM_001100.4:c.990+21G= MANE Select	NP_001091.1:n.990+21G=