Canonical Allele Identifier: CA423755213
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229568436G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432689G>T , CM000663.2:g.229432689G>T GRCh38
NC_000001.10:g.229568436G>T , CM000663.1:g.229568436G>T GRCh37
NC_000001.9:g.227635059G>T NCBI36
NG_006672.1:g.6408C>A , LRG_429:g.6408C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.321C>A ENSP00000355644.4:p.Leu107=
ENST00000684723.1:c.186C>A ENSP00000508084.1:p.Leu62=
ENST00000366683.3:c.321C>A ENSP00000355644.3:p.Leu107=
ENST00000366684.7:c.321C>A MANE Select ENSP00000355645.3:p.Leu107=
NM_001100.3:c.321C>A , LRG_429t1:c.321C>A NP_001091.1:p.Leu107=
NM_001100.4:c.321C>A MANE Select NP_001091.1:p.Leu107=
Search 100 bp 5'
Search 100 bp 3'