Canonical Allele Identifier: CA489655555
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35084754A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792553A>C , CM000677.2:g.34792553A>C GRCh38
NC_000015.9:g.35084754A>C , CM000677.1:g.35084754A>C GRCh37
NC_000015.8:g.32872046A>C NCBI36
NG_007553.1:g.8174T>G , LRG_388:g.8174T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.577T>G (ACTC1)
ENST00000290378.6:c.471T>G (ACTC1) MANE Select ENSP00000290378.4:p.Ser157=
ENST00000647798.1:n.565T>G (ACTC1)
ENST00000648556.1:n.628T>G (ACTC1)
ENST00000650163.1:n.551T>G (ACTC1)
ENST00000290378.4:c.471T>G (ACTC1) ENSP00000290378.4:p.Ser157=
ENST00000557860.1:n.161T>G (ACTC1)
NM_005159.4:c.471T>G , LRG_388t1:c.471T>G (ACTC1) NP_005150.1:p.Ser157=
NR_120329.1:n.299+15122A>C (GJD2-DT)
NM_005159.5:c.471T>G (ACTC1) MANE Select NP_005150.1:p.Ser157=