Canonical Allele Identifier: CA345145572
Gene: ACTA1 HGNC NCBI

Linked Data

gnomAD v4: 1-229431771-G-T
MyVariant Identifiers: chr1:g.229567518G>T (hg19) chr1:g.229431771G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431771G>T , CM000663.2:g.229431771G>T GRCh38
NC_000001.10:g.229567518G>T , CM000663.1:g.229567518G>T GRCh37
NC_000001.9:g.227634141G>T NCBI36
NG_006672.1:g.7326C>A , LRG_429:g.7326C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.940C>A ENSP00000355644.4:p.Arg314Ser
ENST00000684723.1:c.805C>A ENSP00000508084.1:p.Arg269Ser
ENST00000366683.3:c.571C>A ENSP00000355644.3:p.Arg191Ser
ENST00000366684.7:c.940C>A MANE Select ENSP00000355645.3:p.Arg314Ser
NM_001100.3:c.940C>A , LRG_429t1:c.940C>A NP_001091.1:p.Arg314Ser
NM_001100.4:c.940C>A MANE Select NP_001091.1:p.Arg314Ser
Search 100 bp 5'
Search 100 bp 3'