Canonical Allele Identifier: CA2169208873
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792625C= , CM000677.2:g.34792625C= GRCh38
NC_000015.9:g.35084826C= , CM000677.1:g.35084826C= GRCh37
NC_000015.8:g.32872118C= NCBI36
NG_007553.1:g.8102G= , LRG_388:g.8102G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.561-56G= (ACTC1)
ENST00000290378.6:c.455-56G= (ACTC1) MANE Select ENSP00000290378.4:n.455-56G=
ENST00000647798.1:n.549-56G= (ACTC1)
ENST00000648556.1:n.612-56G= (ACTC1)
ENST00000650163.1:n.535-56G= (ACTC1)
ENST00000290378.4:c.455-56G= (ACTC1) ENSP00000290378.4:n.455-56G=
ENST00000557860.1:n.145-56G= (ACTC1)
NM_005159.4:c.455-56G= , LRG_388t1:c.455-56G= (ACTC1) NP_005150.1:n.455-56G=
NR_120329.1:n.299+15194C= (GJD2-DT)
NM_005159.5:c.455-56G= (ACTC1) MANE Select NP_005150.1:n.455-56G=