Canonical Allele Identifier: CA1442859
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs770648114
ExAC: 1:229568204 T / G
gnomAD v2: 1-229568204-T-G
gnomAD v3: 1-229432457-T-G
gnomAD v4: 1-229432457-T-G
MyVariant Identifiers: chr1:g.229568204T>G (hg19) chr1:g.229432457T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432457T>G , CM000663.2:g.229432457T>G GRCh38
NC_000001.10:g.229568204T>G , CM000663.1:g.229568204T>G GRCh37
NC_000001.9:g.227634827T>G NCBI36
NG_006672.1:g.6640A>C , LRG_429:g.6640A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.455-26A>C ENSP00000355644.4:n.455-26A>C
ENST00000684723.1:c.320-26A>C ENSP00000508084.1:n.320-26A>C
ENST00000366683.3:c.455-26A>C ENSP00000355644.3:n.455-26A>C
ENST00000366684.7:c.455-26A>C MANE Select ENSP00000355645.3:n.455-26A>C
NM_001100.3:c.455-26A>C , LRG_429t1:c.455-26A>C NP_001091.1:n.455-26A>C
NM_001100.4:c.455-26A>C MANE Select NP_001091.1:n.455-26A>C
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