Canonical Allele Identifier: CA1226125498
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431810T= , CM000663.2:g.229431810T= GRCh38
NC_000001.10:g.229567557T= , CM000663.1:g.229567557T= GRCh37
NC_000001.9:g.227634180T= NCBI36
NG_006672.1:g.7287A= , LRG_429:g.7287A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.901A= ENSP00000355644.4:p.Met301=
ENST00000684723.1:c.766A= ENSP00000508084.1:p.Met256=
ENST00000366683.3:c.532A= ENSP00000355644.3:p.Met178=
ENST00000366684.7:c.901A= MANE Select ENSP00000355645.3:p.Met301=
NM_001100.3:c.901A= , LRG_429t1:c.901A= NP_001091.1:p.Met301=
NM_001100.4:c.901A= MANE Select NP_001091.1:p.Met301=