Canonical Allele Identifier: CA345145338
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229567482T>G (hg19) chr1:g.229431735T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431735T>G , CM000663.2:g.229431735T>G GRCh38
NC_000001.10:g.229567482T>G , CM000663.1:g.229567482T>G GRCh37
NC_000001.9:g.227634105T>G NCBI36
NG_006672.1:g.7362A>C , LRG_429:g.7362A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.976A>C ENSP00000355644.4:p.Thr326Pro
ENST00000684723.1:c.841A>C ENSP00000508084.1:p.Thr281Pro
ENST00000366683.3:c.607A>C ENSP00000355644.3:p.Thr203Pro
ENST00000366684.7:c.976A>C MANE Select ENSP00000355645.3:p.Thr326Pro
NM_001100.3:c.976A>C , LRG_429t1:c.976A>C NP_001091.1:p.Thr326Pro
NM_001100.4:c.976A>C MANE Select NP_001091.1:p.Thr326Pro
Search 100 bp 5'
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