Canonical Allele Identifier: CA489655557
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35084760C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792559C>G , CM000677.2:g.34792559C>G GRCh38
NC_000015.9:g.35084760C>G , CM000677.1:g.35084760C>G GRCh37
NC_000015.8:g.32872052C>G NCBI36
NG_007553.1:g.8168G>C , LRG_388:g.8168G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.571G>C (ACTC1)
ENST00000290378.6:c.465G>C (ACTC1) MANE Select ENSP00000290378.4:p.Leu155=
ENST00000647798.1:n.559G>C (ACTC1)
ENST00000648556.1:n.622G>C (ACTC1)
ENST00000650163.1:n.545G>C (ACTC1)
ENST00000290378.4:c.465G>C (ACTC1) ENSP00000290378.4:p.Leu155=
ENST00000557860.1:n.155G>C (ACTC1)
NM_005159.4:c.465G>C , LRG_388t1:c.465G>C (ACTC1) NP_005150.1:p.Leu155=
NR_120329.1:n.299+15128C>G (GJD2-DT)
NM_005159.5:c.465G>C (ACTC1) MANE Select NP_005150.1:p.Leu155=