Canonical Allele Identifier: CA1140685062
Gene: ACTA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431937C= , CM000663.2:g.229431937C= GRCh38
NC_000001.10:g.229567684C= , CM000663.1:g.229567684C= GRCh37
NC_000001.9:g.227634307C= NCBI36
NG_006672.1:g.7160G= , LRG_429:g.7160G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.809-35G= ENSP00000355644.4:n.809-35G=
ENST00000684723.1:c.674-35G= ENSP00000508084.1:n.674-35G=
ENST00000366683.3:c.480-75G= ENSP00000355644.3:n.480-75G=
ENST00000366684.7:c.809-35G= MANE Select ENSP00000355645.3:n.809-35G=
NM_001100.3:c.809-35G= , LRG_429t1:c.809-35G= NP_001091.1:n.809-35G=
NM_001100.4:c.809-35G= MANE Select NP_001091.1:n.809-35G=
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