Canonical Allele Identifier: CA2169209948
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34793214C= , CM000677.2:g.34793214C= GRCh38
NC_000015.9:g.35085415C= , CM000677.1:g.35085415C= GRCh37
NC_000015.8:g.32872707C= NCBI36
NG_007553.1:g.7513G= , LRG_388:g.7513G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.560+31G= (ACTC1)
ENST00000290378.6:c.454+31G= (ACTC1) MANE Select ENSP00000290378.4:n.454+31G=
ENST00000647798.1:n.548+84G= (ACTC1)
ENST00000648556.1:n.611+31G= (ACTC1)
ENST00000650163.1:n.534+31G= (ACTC1)
ENST00000290378.4:c.454+31G= (ACTC1) ENSP00000290378.4:n.454+31G=
NM_005159.4:c.454+31G= , LRG_388t1:c.454+31G= (ACTC1) NP_005150.1:n.454+31G=
NR_120329.1:n.299+15783C= (GJD2-DT)
NM_005159.5:c.454+31G= (ACTC1) MANE Select NP_005150.1:n.454+31G=