Canonical Allele Identifier: CA019918
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 177786
ClinVar RCV Id: RCV001508753
dbSNP Id: rs727504323

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792105G>C , CM000677.2:g.34792105G>C GRCh38
NC_000015.9:g.35084306G>C , CM000677.1:g.35084306G>C GRCh37
NC_000015.8:g.32871598G>C NCBI36
NG_007553.1:g.8622C>G , LRG_388:g.8622C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.899C>G (ACTC1)
ENST00000290378.6:c.793C>G (ACTC1) MANE Select ENSP00000290378.4:p.Gln265Glu
ENST00000647798.1:n.887C>G (ACTC1)
ENST00000650163.1:n.873C>G (ACTC1)
ENST00000290378.4:c.793C>G (ACTC1) ENSP00000290378.4:p.Gln265Glu
ENST00000557860.1:n.483C>G (ACTC1)
ENST00000560563.1:n.292C>G (ACTC1)
NM_005159.4:c.793C>G , LRG_388t1:c.793C>G (ACTC1) NP_005150.1:p.Gln265Glu
NR_120329.1:n.299+14674G>C (GJD2-DT)
NM_005159.5:c.793C>G (ACTC1) MANE Select NP_005150.1:p.Gln265Glu