Canonical Allele Identifier: CA345147329

Gene: ACTA1

Linked Data

• COSMIC: COSM3789614
• MyVariant Identifiers: chr1:g.229567907G>C (hg19) ; chr1:g.229432160G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.229432160G>C , CM000663.2:g.229432160G>C	GRCh38
NC_000001.10:g.229567907G>C , CM000663.1:g.229567907G>C	GRCh37
NC_000001.9:g.227634530G>C	NCBI36
NG_006672.1:g.6937C>G , LRG_429:g.6937C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366683.4:c.642C>G	ENSP00000355644.4:p.Ile214Met
ENST00000684723.1:c.507C>G	ENSP00000508084.1:p.Ile169Met
ENST00000366683.3:c.479+247C>G	ENSP00000355644.3:n.479+247C>G
ENST00000366684.7:c.642C>G MANE Select	ENSP00000355645.3:p.Ile214Met
NM_001100.3:c.642C>G , LRG_429t1:c.642C>G	NP_001091.1:p.Ile214Met
NM_001100.4:c.642C>G MANE Select	NP_001091.1:p.Ile214Met