Canonical Allele Identifier: CA345147797
Gene: ACTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432280G>C , CM000663.2:g.229432280G>C GRCh38
NC_000001.10:g.229568027G>C , CM000663.1:g.229568027G>C GRCh37
NC_000001.9:g.227634650G>C NCBI36
NG_006672.1:g.6817C>G , LRG_429:g.6817C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.606C>G ENSP00000355644.4:p.Phe202Leu
ENST00000684723.1:c.471C>G ENSP00000508084.1:p.Phe157Leu
ENST00000366683.3:c.479+127C>G ENSP00000355644.3:n.479+127C>G
ENST00000366684.7:c.606C>G MANE Select ENSP00000355645.3:p.Phe202Leu
NM_001100.3:c.606C>G , LRG_429t1:c.606C>G NP_001091.1:p.Phe202Leu
NM_001100.4:c.606C>G MANE Select NP_001091.1:p.Phe202Leu