Canonical Allele Identifier: CA916422659
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1571892189

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431495dup , CM000663.2:g.229431495dup GRCh38
NC_000001.10:g.229567242dup , CM000663.1:g.229567242dup GRCh37
NC_000001.9:g.227633865dup NCBI36
NG_006672.1:g.7602dup , LRG_429:g.7602dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*4dup ENSP00000355644.4:n.*4dup
ENST00000684723.1:c.*4dup ENSP00000508084.1:n.*4dup
ENST00000366683.3:c.*4dup ENSP00000355644.3:n.*4dup
ENST00000366684.7:c.*4dup MANE Select ENSP00000355645.3:n.*4dup
NM_001100.3:c.*4dup , LRG_429t1:c.*4dup NP_001091.1:n.*4dup
NM_001100.4:c.*4dup MANE Select NP_001091.1:n.*4dup