Canonical Allele Identifier: CA1143376761
Gene: ACTA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432190G= , CM000663.2:g.229432190G= GRCh38
NC_000001.10:g.229567937G= , CM000663.1:g.229567937G= GRCh37
NC_000001.9:g.227634560G= NCBI36
NG_006672.1:g.6907C= , LRG_429:g.6907C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.617-5C= ENSP00000355644.4:n.617-5C=
ENST00000684723.1:c.482-5C= ENSP00000508084.1:n.482-5C=
ENST00000366683.3:c.479+217C= ENSP00000355644.3:n.479+217C=
ENST00000366684.7:c.617-5C= MANE Select ENSP00000355645.3:n.617-5C=
NM_001100.3:c.617-5C= , LRG_429t1:c.617-5C= NP_001091.1:n.617-5C=
NM_001100.4:c.617-5C= MANE Select NP_001091.1:n.617-5C=
Search 100 bp 5'
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