Canonical Allele Identifier: CA423755129
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1254930596
MyVariant Identifiers: chr1:g.229568168C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432421C>G , CM000663.2:g.229432421C>G GRCh38
NC_000001.10:g.229568168C>G , CM000663.1:g.229568168C>G GRCh37
NC_000001.9:g.227634791C>G NCBI36
NG_006672.1:g.6676G>C , LRG_429:g.6676G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.465G>C ENSP00000355644.4:p.Leu155=
ENST00000684723.1:c.330G>C ENSP00000508084.1:p.Leu110=
ENST00000366683.3:c.465G>C ENSP00000355644.3:p.Leu155=
ENST00000366684.7:c.465G>C MANE Select ENSP00000355645.3:p.Leu155=
NM_001100.3:c.465G>C , LRG_429t1:c.465G>C NP_001091.1:p.Leu155=
NM_001100.4:c.465G>C MANE Select NP_001091.1:p.Leu155=
Search 100 bp 5'
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