Canonical Allele Identifier: CA1146199362
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432587C= , CM000663.2:g.229432587C= GRCh38
NC_000001.10:g.229568334C= , CM000663.1:g.229568334C= GRCh37
NC_000001.9:g.227634957C= NCBI36
NG_006672.1:g.6510G= , LRG_429:g.6510G=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.423G= ENSP00000355644.4:p.Val141=
ENST00000684723.1:c.288G= ENSP00000508084.1:p.Val96=
ENST00000366683.3:c.423G= ENSP00000355644.3:p.Val141=
ENST00000366684.7:c.423G= MANE Select ENSP00000355645.3:p.Val141=
NM_001100.3:c.423G= , LRG_429t1:c.423G= NP_001091.1:p.Val141=
NM_001100.4:c.423G= MANE Select NP_001091.1:p.Val141=