Canonical Allele Identifier: CA423755000
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229567796G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432049G>T , CM000663.2:g.229432049G>T GRCh38
NC_000001.10:g.229567796G>T , CM000663.1:g.229567796G>T GRCh37
NC_000001.9:g.227634419G>T NCBI36
NG_006672.1:g.7048C>A , LRG_429:g.7048C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.753C>A ENSP00000355644.4:p.Thr251=
ENST00000684723.1:c.618C>A ENSP00000508084.1:p.Thr206=
ENST00000366683.3:c.480-187C>A ENSP00000355644.3:n.480-187C>A
ENST00000366684.7:c.753C>A MANE Select ENSP00000355645.3:p.Thr251=
NM_001100.3:c.753C>A , LRG_429t1:c.753C>A NP_001091.1:p.Thr251=
NM_001100.4:c.753C>A MANE Select NP_001091.1:p.Thr251=
Search 100 bp 5'
Search 100 bp 3'