Canonical Allele Identifier: CA1226125578
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431945_229431946delinsCG , CM000663.2:g.229431945_229431946delinsCG GRCh38
NC_000001.10:g.229567692_229567693delinsCG , CM000663.1:g.229567692_229567693delinsCG GRCh37
NC_000001.9:g.227634315_227634316delinsCG NCBI36
NG_006672.1:g.7151_7152delinsCG , LRG_429:g.7151_7152delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.809-44_809-43delinsCG ENSP00000355644.4:n.809-44_809-43delinsCG
ENST00000684723.1:c.674-44_674-43delinsCG ENSP00000508084.1:n.674-44_674-43delinsCG
ENST00000366683.3:c.480-84_480-83delinsCG ENSP00000355644.3:n.480-84_480-83delinsCG
ENST00000366684.7:c.809-44_809-43delinsCG MANE Select ENSP00000355645.3:n.809-44_809-43delinsCG
NM_001100.3:c.809-44_809-43delinsCG , LRG_429t1:c.809-44_809-43delinsCG NP_001091.1:n.809-44_809-43delinsCG
NM_001100.4:c.809-44_809-43delinsCG MANE Select NP_001091.1:n.809-44_809-43delinsCG