Canonical Allele Identifier: CA489655417
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

dbSNP Id: rs1595760921
MyVariant Identifiers: chr15:g.35084628G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792427G>C , CM000677.2:g.34792427G>C GRCh38
NC_000015.9:g.35084628G>C , CM000677.1:g.35084628G>C GRCh37
NC_000015.8:g.32871920G>C NCBI36
NG_007553.1:g.8300C>G , LRG_388:g.8300C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.703C>G (ACTC1)
ENST00000290378.6:c.597C>G (ACTC1) MANE Select ENSP00000290378.4:p.Gly199=
ENST00000647798.1:n.691C>G (ACTC1)
ENST00000648556.1:n.754C>G (ACTC1)
ENST00000650163.1:n.677C>G (ACTC1)
ENST00000290378.4:c.597C>G (ACTC1) ENSP00000290378.4:p.Gly199=
ENST00000557860.1:n.287C>G (ACTC1)
ENST00000560563.1:n.96C>G (ACTC1)
NM_005159.4:c.597C>G , LRG_388t1:c.597C>G (ACTC1) NP_005150.1:p.Gly199=
NR_120329.1:n.299+14996G>C (GJD2-DT)
NM_005159.5:c.597C>G (ACTC1) MANE Select NP_005150.1:p.Gly199=
Search 100 bp 5'
Search 100 bp 3'