Canonical Allele Identifier: CA1226125823
Gene: ACTA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432497G= , CM000663.2:g.229432497G= GRCh38
NC_000001.10:g.229568244G= , CM000663.1:g.229568244G= GRCh37
NC_000001.9:g.227634867G= NCBI36
NG_006672.1:g.6600C= , LRG_429:g.6600C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.454+59C= ENSP00000355644.4:n.454+59C=
ENST00000684723.1:c.319+59C= ENSP00000508084.1:n.319+59C=
ENST00000366683.3:c.454+59C= ENSP00000355644.3:n.454+59C=
ENST00000366684.7:c.454+59C= MANE Select ENSP00000355645.3:n.454+59C=
NM_001100.3:c.454+59C= , LRG_429t1:c.454+59C= NP_001091.1:n.454+59C=
NM_001100.4:c.454+59C= MANE Select NP_001091.1:n.454+59C=
Search 100 bp 5'
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