Canonical Allele Identifier: CA2748068638
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431929_229431930insTAAGC , CM000663.2:g.229431929_229431930insTAAGC GRCh38
NC_000001.10:g.229567676_229567677insTAAGC , CM000663.1:g.229567676_229567677insTAAGC GRCh37
NC_000001.9:g.227634299_227634300insTAAGC NCBI36
NG_006672.1:g.7170_7171insTAGCT , LRG_429:g.7170_7171insTAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.809-25_809-24insTAGCT ENSP00000355644.4:n.809-25_809-24insTAGCT
ENST00000684723.1:c.674-25_674-24insTAGCT ENSP00000508084.1:n.674-25_674-24insTAGCT
ENST00000366683.3:c.480-65_480-64insTAGCT ENSP00000355644.3:n.480-65_480-64insTAGCT
ENST00000366684.7:c.809-25_809-24insTAGCT MANE Select ENSP00000355645.3:n.809-25_809-24insTAGCT
NM_001100.3:c.809-25_809-24insTAGCT , LRG_429t1:c.809-25_809-24insTAGCT NP_001091.1:n.809-25_809-24insTAGCT
NM_001100.4:c.809-25_809-24insTAGCT MANE Select NP_001091.1:n.809-25_809-24insTAGCT