Canonical Allele Identifier: CA2169208426
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792446T= , CM000677.2:g.34792446T= GRCh38
NC_000015.9:g.35084647T= , CM000677.1:g.35084647T= GRCh37
NC_000015.8:g.32871939T= NCBI36
NG_007553.1:g.8281A= , LRG_388:g.8281A=

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.684A= (ACTC1)
ENST00000290378.6:c.578A= (ACTC1) MANE Select ENSP00000290378.4:p.Lys193=
ENST00000647798.1:n.672A= (ACTC1)
ENST00000648556.1:n.735A= (ACTC1)
ENST00000650163.1:n.658A= (ACTC1)
ENST00000290378.4:c.578A= (ACTC1) ENSP00000290378.4:p.Lys193=
ENST00000557860.1:n.268A= (ACTC1)
ENST00000560563.1:n.77A= (ACTC1)
NM_005159.4:c.578A= , LRG_388t1:c.578A= (ACTC1) NP_005150.1:p.Lys193=
NR_120329.1:n.299+15015T= (GJD2-DT)
NM_005159.5:c.578A= (ACTC1) MANE Select NP_005150.1:p.Lys193=