Canonical Allele Identifier: CA2169208226
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

dbSNP Id: rs1891722229

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792355G>C , CM000677.2:g.34792355G>C GRCh38
NC_000015.9:g.35084556G>C , CM000677.1:g.35084556G>C GRCh37
NC_000015.8:g.32871848G>C NCBI36
NG_007553.1:g.8372C>G , LRG_388:g.8372C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.722+53C>G (ACTC1)
ENST00000290378.6:c.616+53C>G (ACTC1) MANE Select ENSP00000290378.4:n.616+53C>G
ENST00000647798.1:n.710+53C>G (ACTC1)
ENST00000648556.1:n.773+53C>G (ACTC1)
ENST00000650163.1:n.696+53C>G (ACTC1)
ENST00000290378.4:c.616+53C>G (ACTC1) ENSP00000290378.4:n.616+53C>G
ENST00000557860.1:n.306+53C>G (ACTC1)
ENST00000560563.1:n.115+53C>G (ACTC1)
NM_005159.4:c.616+53C>G , LRG_388t1:c.616+53C>G (ACTC1) NP_005150.1:n.616+53C>G
NR_120329.1:n.299+14924G>C (GJD2-DT)
NM_005159.5:c.616+53C>G (ACTC1) MANE Select NP_005150.1:n.616+53C>G