Canonical Allele Identifier: CA2573053985
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 1319899
ClinVar RCV Id: RCV003238145
dbSNP Id: rs2140430900

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792469_34792474del , CM000677.2:g.34792469_34792474del GRCh38
NC_000015.9:g.35084670_35084675del , CM000677.1:g.35084670_35084675del GRCh37
NC_000015.8:g.32871962_32871967del NCBI36
NG_007553.1:g.8254_8259del , LRG_388:g.8254_8259del

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.657_662del (ACTC1)
ENST00000290378.6:c.551_556del (ACTC1) MANE Select ENSP00000290378.4:p.Gly184_Arg185del
ENST00000647798.1:n.645_650del (ACTC1)
ENST00000648556.1:n.708_713del (ACTC1)
ENST00000650163.1:n.631_636del (ACTC1)
ENST00000290378.4:c.551_556del (ACTC1) ENSP00000290378.4:p.Gly184_Arg185del
ENST00000557860.1:n.241_246del (ACTC1)
ENST00000560563.1:n.50_55del (ACTC1)
NM_005159.4:c.551_556del , LRG_388t1:c.551_556del (ACTC1) NP_005150.1:p.Gly184_Arg185del
NR_120329.1:n.299+15038_299+15043del (GJD2-DT)
NM_005159.5:c.551_556del (ACTC1) MANE Select NP_005150.1:p.Gly184_Arg185del