Canonical Allele Identifier: CA489655550
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

dbSNP Id: rs1595760995
MyVariant Identifiers: chr15:g.35084751C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792550C>G , CM000677.2:g.34792550C>G GRCh38
NC_000015.9:g.35084751C>G , CM000677.1:g.35084751C>G GRCh37
NC_000015.8:g.32872043C>G NCBI36
NG_007553.1:g.8177G>C , LRG_388:g.8177G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.580G>C (ACTC1)
ENST00000290378.6:c.474G>C (ACTC1) MANE Select ENSP00000290378.4:p.Gly158=
ENST00000647798.1:n.568G>C (ACTC1)
ENST00000648556.1:n.631G>C (ACTC1)
ENST00000650163.1:n.554G>C (ACTC1)
ENST00000290378.4:c.474G>C (ACTC1) ENSP00000290378.4:p.Gly158=
ENST00000557860.1:n.164G>C (ACTC1)
NM_005159.4:c.474G>C , LRG_388t1:c.474G>C (ACTC1) NP_005150.1:p.Gly158=
NR_120329.1:n.299+15119C>G (GJD2-DT)
NM_005159.5:c.474G>C (ACTC1) MANE Select NP_005150.1:p.Gly158=