Canonical Allele Identifier: CA2169208035
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792275C= , CM000677.2:g.34792275C= GRCh38
NC_000015.9:g.35084476C= , CM000677.1:g.35084476C= GRCh37
NC_000015.8:g.32871768C= NCBI36
NG_007553.1:g.8452G= , LRG_388:g.8452G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.729G= (ACTC1)
ENST00000290378.6:c.623G= (ACTC1) MANE Select ENSP00000290378.4:p.Arg208=
ENST00000647798.1:n.717G= (ACTC1)
ENST00000648556.1:n.780G= (ACTC1)
ENST00000650163.1:n.703G= (ACTC1)
ENST00000290378.4:c.623G= (ACTC1) ENSP00000290378.4:p.Arg208=
ENST00000557860.1:n.313G= (ACTC1)
ENST00000560563.1:n.122G= (ACTC1)
NM_005159.4:c.623G= , LRG_388t1:c.623G= (ACTC1) NP_005150.1:p.Arg208=
NR_120329.1:n.299+14844C= (GJD2-DT)
NM_005159.5:c.623G= (ACTC1) MANE Select NP_005150.1:p.Arg208=