Canonical Allele Identifier: CA1226125603
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431976A= , CM000663.2:g.229431976A= GRCh38
NC_000001.10:g.229567723A= , CM000663.1:g.229567723A= GRCh37
NC_000001.9:g.227634346A= NCBI36
NG_006672.1:g.7121T= , LRG_429:g.7121T=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.808+18T= ENSP00000355644.4:n.808+18T=
ENST00000684723.1:c.673+18T= ENSP00000508084.1:n.673+18T=
ENST00000366683.3:c.480-114T= ENSP00000355644.3:n.480-114T=
ENST00000366684.7:c.808+18T= MANE Select ENSP00000355645.3:n.808+18T=
NM_001100.3:c.808+18T= , LRG_429t1:c.808+18T= NP_001091.1:n.808+18T=
NM_001100.4:c.808+18T= MANE Select NP_001091.1:n.808+18T=