Canonical Allele Identifier: CA345147344
Gene: ACTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635438
ClinVar RCV Id: RCV003410534
MyVariant Identifiers: chr1:g.229567909T>C (hg19) chr1:g.229432162T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432162T>C , CM000663.2:g.229432162T>C GRCh38
NC_000001.10:g.229567909T>C , CM000663.1:g.229567909T>C GRCh37
NC_000001.9:g.227634532T>C NCBI36
NG_006672.1:g.6935A>G , LRG_429:g.6935A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.640A>G ENSP00000355644.4:p.Ile214Val
ENST00000684723.1:c.505A>G ENSP00000508084.1:p.Ile169Val
ENST00000366683.3:c.479+245A>G ENSP00000355644.3:n.479+245A>G
ENST00000366684.7:c.640A>G MANE Select ENSP00000355645.3:p.Ile214Val
NM_001100.3:c.640A>G , LRG_429t1:c.640A>G NP_001091.1:p.Ile214Val
NM_001100.4:c.640A>G MANE Select NP_001091.1:p.Ile214Val
Search 100 bp 5'
Search 100 bp 3'