Canonical Allele Identifier: CA489655502
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35084715G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792514G>T , CM000677.2:g.34792514G>T GRCh38
NC_000015.9:g.35084715G>T , CM000677.1:g.35084715G>T GRCh37
NC_000015.8:g.32872007G>T NCBI36
NG_007553.1:g.8213C>A , LRG_388:g.8213C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.616C>A (ACTC1)
ENST00000290378.6:c.510C>A (ACTC1) MANE Select ENSP00000290378.4:p.Gly170=
ENST00000647798.1:n.604C>A (ACTC1)
ENST00000648556.1:n.667C>A (ACTC1)
ENST00000650163.1:n.590C>A (ACTC1)
ENST00000290378.4:c.510C>A (ACTC1) ENSP00000290378.4:p.Gly170=
ENST00000557860.1:n.200C>A (ACTC1)
ENST00000560563.1:n.9C>A (ACTC1)
NM_005159.4:c.510C>A , LRG_388t1:c.510C>A (ACTC1) NP_005150.1:p.Gly170=
NR_120329.1:n.299+15083G>T (GJD2-DT)
NM_005159.5:c.510C>A (ACTC1) MANE Select NP_005150.1:p.Gly170=