Canonical Allele Identifier: CA1142218806
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432971G= , CM000663.2:g.229432971G= GRCh38
NC_000001.10:g.229568718G= , CM000663.1:g.229568718G= GRCh37
NC_000001.9:g.227635341G= NCBI36
NG_006672.1:g.6126C= , LRG_429:g.6126C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.129+16C= ENSP00000355644.4:n.129+16C=
ENST00000684723.1:c.-6-91C= ENSP00000508084.1:n.-6-91C=
ENST00000366683.3:c.129+16C= ENSP00000355644.3:n.129+16C=
ENST00000366684.7:c.129+16C= MANE Select ENSP00000355645.3:n.129+16C=
NM_001100.3:c.129+16C= , LRG_429t1:c.129+16C= NP_001091.1:n.129+16C=
NM_001100.4:c.129+16C= MANE Select NP_001091.1:n.129+16C=