Canonical Allele Identifier: CA489655444
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 919357
ClinVar RCV Id: RCV001177491
dbSNP Id: rs1891724406
MyVariant Identifiers: chr15:g.35084667G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792466G>A , CM000677.2:g.34792466G>A GRCh38
NC_000015.9:g.35084667G>A , CM000677.1:g.35084667G>A GRCh37
NC_000015.8:g.32871959G>A NCBI36
NG_007553.1:g.8261C>T , LRG_388:g.8261C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.664C>T (ACTC1)
ENST00000290378.6:c.558C>T (ACTC1) MANE Select ENSP00000290378.4:p.Asp186=
ENST00000647798.1:n.652C>T (ACTC1)
ENST00000648556.1:n.715C>T (ACTC1)
ENST00000650163.1:n.638C>T (ACTC1)
ENST00000290378.4:c.558C>T (ACTC1) ENSP00000290378.4:p.Asp186=
ENST00000557860.1:n.248C>T (ACTC1)
ENST00000560563.1:n.57C>T (ACTC1)
NM_005159.4:c.558C>T , LRG_388t1:c.558C>T (ACTC1) NP_005150.1:p.Asp186=
NR_120329.1:n.299+15035G>A (GJD2-DT)
NM_005159.5:c.558C>T (ACTC1) MANE Select NP_005150.1:p.Asp186=