Canonical Allele Identifier: CA268663301
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 478616
ClinVar RCV Id: RCV002330988
dbSNP Id: rs922191208
gnomAD v3: 15-34793276-C-T
gnomAD v4: 15-34793276-C-T
MyVariant Identifiers: chr15:g.35085477C>T (hg19) chr15:g.34793276C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34793276C>T , CM000677.2:g.34793276C>T GRCh38
NC_000015.9:g.35085477C>T , CM000677.1:g.35085477C>T GRCh37
NC_000015.8:g.32872769C>T NCBI36
NG_007553.1:g.7451G>A , LRG_388:g.7451G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.529G>A (ACTC1)
ENST00000290378.6:c.423G>A (ACTC1) MANE Select ENSP00000290378.4:p.Val141=
ENST00000647798.1:n.548+22G>A (ACTC1)
ENST00000648556.1:n.580G>A (ACTC1)
ENST00000650163.1:n.503G>A (ACTC1)
ENST00000290378.4:c.423G>A (ACTC1) ENSP00000290378.4:p.Val141=
NM_005159.4:c.423G>A , LRG_388t1:c.423G>A (ACTC1) NP_005150.1:p.Val141=
NR_120329.1:n.299+15845C>T (GJD2-DT)
NM_005159.5:c.423G>A (ACTC1) MANE Select NP_005150.1:p.Val141=
Search 100 bp 5'
Search 100 bp 3'