Canonical Allele Identifier: CA489419601
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35084328G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792127G>A , CM000677.2:g.34792127G>A GRCh38
NC_000015.9:g.35084328G>A , CM000677.1:g.35084328G>A GRCh37
NC_000015.8:g.32871620G>A NCBI36
NG_007553.1:g.8600C>T , LRG_388:g.8600C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.877C>T (ACTC1)
ENST00000290378.6:c.771C>T (ACTC1) MANE Select ENSP00000290378.4:p.Phe257=
ENST00000647798.1:n.865C>T (ACTC1)
ENST00000650163.1:n.851C>T (ACTC1)
ENST00000290378.4:c.771C>T (ACTC1) ENSP00000290378.4:p.Phe257=
ENST00000557860.1:n.461C>T (ACTC1)
ENST00000560563.1:n.270C>T (ACTC1)
NM_005159.4:c.771C>T , LRG_388t1:c.771C>T (ACTC1) NP_005150.1:p.Phe257=
NR_120329.1:n.299+14696G>A (GJD2-DT)
NM_005159.5:c.771C>T (ACTC1) MANE Select NP_005150.1:p.Phe257=