Canonical Allele Identifier: CA1226125674
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432187T= , CM000663.2:g.229432187T= GRCh38
NC_000001.10:g.229567934T= , CM000663.1:g.229567934T= GRCh37
NC_000001.9:g.227634557T= NCBI36
NG_006672.1:g.6910A= , LRG_429:g.6910A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.617-2A= ENSP00000355644.4:n.617-2A=
ENST00000684723.1:c.482-2A= ENSP00000508084.1:n.482-2A=
ENST00000366683.3:c.479+220A= ENSP00000355644.3:n.479+220A=
ENST00000366684.7:c.617-2A= MANE Select ENSP00000355645.3:n.617-2A=
NM_001100.3:c.617-2A= , LRG_429t1:c.617-2A= NP_001091.1:n.617-2A=
NM_001100.4:c.617-2A= MANE Select NP_001091.1:n.617-2A=