Canonical Allele Identifier: CA345149205
Gene: ACTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1409843
ClinVar RCV Id: RCV001939933
dbSNP Id: rs1553255482
MyVariant Identifiers: chr1:g.229568332A>C (hg19) chr1:g.229432585A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432585A>C , CM000663.2:g.229432585A>C GRCh38
NC_000001.10:g.229568332A>C , CM000663.1:g.229568332A>C GRCh37
NC_000001.9:g.227634955A>C NCBI36
NG_006672.1:g.6512T>G , LRG_429:g.6512T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.425T>G ENSP00000355644.4:p.Leu142Arg
ENST00000684723.1:c.290T>G ENSP00000508084.1:p.Leu97Arg
ENST00000366683.3:c.425T>G ENSP00000355644.3:p.Leu142Arg
ENST00000366684.7:c.425T>G MANE Select ENSP00000355645.3:p.Leu142Arg
NM_001100.3:c.425T>G , LRG_429t1:c.425T>G NP_001091.1:p.Leu142Arg
NM_001100.4:c.425T>G MANE Select NP_001091.1:p.Leu142Arg
Search 100 bp 5'
Search 100 bp 3'