Canonical Allele Identifier: CA2169208082
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792288A= , CM000677.2:g.34792288A= GRCh38
NC_000015.9:g.35084489A= , CM000677.1:g.35084489A= GRCh37
NC_000015.8:g.32871781A= NCBI36
NG_007553.1:g.8439T= , LRG_388:g.8439T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.723-7T= (ACTC1)
ENST00000290378.6:c.617-7T= (ACTC1) MANE Select ENSP00000290378.4:n.617-7T=
ENST00000647798.1:n.711-7T= (ACTC1)
ENST00000648556.1:n.774-7T= (ACTC1)
ENST00000650163.1:n.697-7T= (ACTC1)
ENST00000290378.4:c.617-7T= (ACTC1) ENSP00000290378.4:n.617-7T=
ENST00000557860.1:n.307-7T= (ACTC1)
ENST00000560563.1:n.116-7T= (ACTC1)
NM_005159.4:c.617-7T= , LRG_388t1:c.617-7T= (ACTC1) NP_005150.1:n.617-7T=
NR_120329.1:n.299+14857A= (GJD2-DT)
NM_005159.5:c.617-7T= (ACTC1) MANE Select NP_005150.1:n.617-7T=