Canonical Allele Identifier: CA489420784
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

dbSNP Id: rs1403653818
COSMIC: COSM127253
MyVariant Identifiers: chr15:g.35086908C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34794707C>A , CM000677.2:g.34794707C>A GRCh38
NC_000015.9:g.35086908C>A , CM000677.1:g.35086908C>A GRCh37
NC_000015.8:g.32874200C>A NCBI36
NG_007553.1:g.6020G>T , LRG_388:g.6020G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.208G>T (ACTC1)
ENST00000290378.6:c.102G>T (ACTC1) MANE Select ENSP00000290378.4:p.Pro34=
ENST00000290378.4:c.102G>T (ACTC1) ENSP00000290378.4:p.Pro34=
NM_005159.4:c.102G>T , LRG_388t1:c.102G>T (ACTC1) NP_005150.1:p.Pro34=
NR_120329.1:n.300-15789C>A (GJD2-DT)
NM_005159.5:c.102G>T (ACTC1) MANE Select NP_005150.1:p.Pro34=