Canonical Allele Identifier: CA345145047
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229567390C>G (hg19) chr1:g.229431643C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431643C>G , CM000663.2:g.229431643C>G GRCh38
NC_000001.10:g.229567390C>G , CM000663.1:g.229567390C>G GRCh37
NC_000001.9:g.227634013C>G NCBI36
NG_006672.1:g.7454G>C , LRG_429:g.7454G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.991-79G>C ENSP00000355644.4:n.991-79G>C
ENST00000684723.1:c.856-1G>C ENSP00000508084.1:n.856-1G>C
ENST00000366683.3:c.622-1G>C ENSP00000355644.3:n.622-1G>C
ENST00000366684.7:c.991-1G>C MANE Select ENSP00000355645.3:n.991-1G>C
NM_001100.3:c.991-1G>C , LRG_429t1:c.991-1G>C NP_001091.1:n.991-1G>C
NM_001100.4:c.991-1G>C MANE Select NP_001091.1:n.991-1G>C
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