Canonical Allele Identifier: CA345146116
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229567616T>G (hg19) chr1:g.229431869T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431869T>G , CM000663.2:g.229431869T>G GRCh38
NC_000001.10:g.229567616T>G , CM000663.1:g.229567616T>G GRCh37
NC_000001.9:g.227634239T>G NCBI36
NG_006672.1:g.7228A>C , LRG_429:g.7228A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.842A>C ENSP00000355644.4:p.Tyr281Ser
ENST00000684723.1:c.707A>C ENSP00000508084.1:p.Tyr236Ser
ENST00000366683.3:c.480-7A>C ENSP00000355644.3:n.480-7A>C
ENST00000366684.7:c.842A>C MANE Select ENSP00000355645.3:p.Tyr281Ser
NM_001100.3:c.842A>C , LRG_429t1:c.842A>C NP_001091.1:p.Tyr281Ser
NM_001100.4:c.842A>C MANE Select NP_001091.1:p.Tyr281Ser
Search 100 bp 5'
Search 100 bp 3'