Canonical Allele Identifier: CA1145165738
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431981G= , CM000663.2:g.229431981G= GRCh38
NC_000001.10:g.229567728G= , CM000663.1:g.229567728G= GRCh37
NC_000001.9:g.227634351G= NCBI36
NG_006672.1:g.7116C= , LRG_429:g.7116C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.808+13C= ENSP00000355644.4:n.808+13C=
ENST00000684723.1:c.673+13C= ENSP00000508084.1:n.673+13C=
ENST00000366683.3:c.480-119C= ENSP00000355644.3:n.480-119C=
ENST00000366684.7:c.808+13C= MANE Select ENSP00000355645.3:n.808+13C=
NM_001100.3:c.808+13C= , LRG_429t1:c.808+13C= NP_001091.1:n.808+13C=
NM_001100.4:c.808+13C= MANE Select NP_001091.1:n.808+13C=