Canonical Allele Identifier: CA2169206628
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34791545C= , CM000677.2:g.34791545C= GRCh38
NC_000015.9:g.35083746C= , CM000677.1:g.35083746C= GRCh37
NC_000015.8:g.32871038C= NCBI36
NG_007553.1:g.9182G= , LRG_388:g.9182G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.1459G= (ACTC1)
ENST00000290378.6:c.809-250G= (ACTC1) MANE Select ENSP00000290378.4:n.809-250G=
ENST00000647798.1:n.903-250G= (ACTC1)
ENST00000650163.1:n.889-250G= (ACTC1)
ENST00000290378.4:c.809-250G= (ACTC1) ENSP00000290378.4:n.809-250G=
ENST00000557860.1:n.499-250G= (ACTC1)
NM_005159.4:c.809-250G= , LRG_388t1:c.809-250G= (ACTC1) NP_005150.1:n.809-250G=
NR_120329.1:n.299+14114C= (GJD2-DT)
NM_005159.5:c.809-250G= (ACTC1) MANE Select NP_005150.1:n.809-250G=