Canonical Allele Identifier: CA2169208257
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792376C= , CM000677.2:g.34792376C= GRCh38
NC_000015.9:g.35084577C= , CM000677.1:g.35084577C= GRCh37
NC_000015.8:g.32871869C= NCBI36
NG_007553.1:g.8351G= , LRG_388:g.8351G=

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.722+32G= (ACTC1)
ENST00000290378.6:c.616+32G= (ACTC1) MANE Select ENSP00000290378.4:n.616+32G=
ENST00000647798.1:n.710+32G= (ACTC1)
ENST00000648556.1:n.773+32G= (ACTC1)
ENST00000650163.1:n.696+32G= (ACTC1)
ENST00000290378.4:c.616+32G= (ACTC1) ENSP00000290378.4:n.616+32G=
ENST00000557860.1:n.306+32G= (ACTC1)
ENST00000560563.1:n.115+32G= (ACTC1)
NM_005159.4:c.616+32G= , LRG_388t1:c.616+32G= (ACTC1) NP_005150.1:n.616+32G=
NR_120329.1:n.299+14945C= (GJD2-DT)
NM_005159.5:c.616+32G= (ACTC1) MANE Select NP_005150.1:n.616+32G=