Canonical Allele Identifier: CA391631151
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 1437697
ClinVar RCV Id: RCV001934076
dbSNP Id: rs2140431025

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792551C>T , CM000677.2:g.34792551C>T GRCh38
NC_000015.9:g.35084752C>T , CM000677.1:g.35084752C>T GRCh37
NC_000015.8:g.32872044C>T NCBI36
NG_007553.1:g.8176G>A , LRG_388:g.8176G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.579G>A (ACTC1)
ENST00000290378.6:c.473G>A (ACTC1) MANE Select ENSP00000290378.4:p.Gly158Glu
ENST00000647798.1:n.567G>A (ACTC1)
ENST00000648556.1:n.630G>A (ACTC1)
ENST00000650163.1:n.553G>A (ACTC1)
ENST00000290378.4:c.473G>A (ACTC1) ENSP00000290378.4:p.Gly158Glu
ENST00000557860.1:n.163G>A (ACTC1)
NM_005159.4:c.473G>A , LRG_388t1:c.473G>A (ACTC1) NP_005150.1:p.Gly158Glu
NR_120329.1:n.299+15120C>T (GJD2-DT)
NM_005159.5:c.473G>A (ACTC1) MANE Select NP_005150.1:p.Gly158Glu