Canonical Allele Identifier: CA391632078
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 3224600
ClinVar RCV Id: RCV004521291
MyVariant Identifiers: chr15:g.35085722C>A (hg19) chr15:g.34793521C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34793521C>A , CM000677.2:g.34793521C>A GRCh38
NC_000015.9:g.35085722C>A , CM000677.1:g.35085722C>A GRCh37
NC_000015.8:g.32873014C>A NCBI36
NG_007553.1:g.7206G>T , LRG_388:g.7206G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.284G>T (ACTC1)
ENST00000290378.6:c.178G>T (ACTC1) MANE Select ENSP00000290378.4:p.Ala60Ser
ENST00000647798.1:n.325G>T (ACTC1)
ENST00000648556.1:n.335G>T (ACTC1)
ENST00000650163.1:n.258G>T (ACTC1)
ENST00000290378.4:c.178G>T (ACTC1) ENSP00000290378.4:p.Ala60Ser
NM_005159.4:c.178G>T , LRG_388t1:c.178G>T (ACTC1) NP_005150.1:p.Ala60Ser
NR_120329.1:n.299+16090C>A (GJD2-DT)
NM_005159.5:c.178G>T (ACTC1) MANE Select NP_005150.1:p.Ala60Ser
Search 100 bp 5'
Search 100 bp 3'