Canonical Allele Identifier: CA345146368
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229431938del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431941del , CM000663.2:g.229431941del GRCh38
NC_000001.10:g.229567688del , CM000663.1:g.229567688del GRCh37
NC_000001.9:g.227634311del NCBI36
NG_006672.1:g.7159del , LRG_429:g.7159del

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.809-36del ENSP00000355644.4:n.809-36del
ENST00000684723.1:c.674-36del ENSP00000508084.1:n.674-36del
ENST00000366683.3:c.480-76del ENSP00000355644.3:n.480-76del
ENST00000366684.7:c.809-36del MANE Select ENSP00000355645.3:n.809-36del
NM_001100.3:c.809-36del , LRG_429t1:c.809-36del NP_001091.1:n.809-36del
NM_001100.4:c.809-36del MANE Select NP_001091.1:n.809-36del