Canonical Allele Identifier: CA1145913200
Gene: ACTA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431991C= , CM000663.2:g.229431991C= GRCh38
NC_000001.10:g.229567738C= , CM000663.1:g.229567738C= GRCh37
NC_000001.9:g.227634361C= NCBI36
NG_006672.1:g.7106G= , LRG_429:g.7106G=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.808+3G= ENSP00000355644.4:n.808+3G=
ENST00000684723.1:c.673+3G= ENSP00000508084.1:n.673+3G=
ENST00000366683.3:c.480-129G= ENSP00000355644.3:n.480-129G=
ENST00000366684.7:c.808+3G= MANE Select ENSP00000355645.3:n.808+3G=
NM_001100.3:c.808+3G= , LRG_429t1:c.808+3G= NP_001091.1:n.808+3G=
NM_001100.4:c.808+3G= MANE Select NP_001091.1:n.808+3G=
Search 100 bp 5'
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