Canonical Allele Identifier: CA2169205581
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34791218A= , CM000677.2:g.34791218A= GRCh38
NC_000015.9:g.35083419A= , CM000677.1:g.35083419A= GRCh37
NC_000015.8:g.32870711A= NCBI36
NG_007553.1:g.9509T= , LRG_388:g.9509T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.1786T= (ACTC1)
ENST00000290378.6:c.886T= (ACTC1) MANE Select ENSP00000290378.4:p.Tyr296=
ENST00000647798.1:n.980T= (ACTC1)
ENST00000650163.1:n.966T= (ACTC1)
ENST00000290378.4:c.886T= (ACTC1) ENSP00000290378.4:p.Tyr296=
ENST00000557860.1:n.576T= (ACTC1)
NM_005159.4:c.886T= , LRG_388t1:c.886T= (ACTC1) NP_005150.1:p.Tyr296=
NR_120329.1:n.299+13787A= (GJD2-DT)
NM_005159.5:c.886T= (ACTC1) MANE Select NP_005150.1:p.Tyr296=