Canonical Allele Identifier: CA732579140
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1458028822
gnomAD v4: 1-229431445-C-A
MyVariant Identifiers: chr1:g.229567192C>A (hg19) chr1:g.229431445C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431445C>A , CM000663.2:g.229431445C>A GRCh38
NC_000001.10:g.229567192C>A , CM000663.1:g.229567192C>A GRCh37
NC_000001.9:g.227633815C>A NCBI36
NG_006672.1:g.7652G>T , LRG_429:g.7652G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.*54G>T ENSP00000355644.4:n.*54G>T
ENST00000684723.1:c.*54G>T ENSP00000508084.1:n.*54G>T
ENST00000366683.3:c.*54G>T ENSP00000355644.3:n.*54G>T
ENST00000366684.7:c.*54G>T MANE Select ENSP00000355645.3:n.*54G>T
NM_001100.3:c.*54G>T , LRG_429t1:c.*54G>T NP_001091.1:n.*54G>T
NM_001100.4:c.*54G>T MANE Select NP_001091.1:n.*54G>T
Search 100 bp 5'
Search 100 bp 3'