Canonical Allele Identifier: CA489419446
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35084292A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792091A>G , CM000677.2:g.34792091A>G GRCh38
NC_000015.9:g.35084292A>G , CM000677.1:g.35084292A>G GRCh37
NC_000015.8:g.32871584A>G NCBI36
NG_007553.1:g.8636T>C , LRG_388:g.8636T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000560563.2:n.913T>C (ACTC1)
ENST00000290378.6:c.807T>C (ACTC1) MANE Select ENSP00000290378.4:p.Ile269=
ENST00000647798.1:n.901T>C (ACTC1)
ENST00000650163.1:n.887T>C (ACTC1)
ENST00000290378.4:c.807T>C (ACTC1) ENSP00000290378.4:p.Ile269=
ENST00000557860.1:n.497T>C (ACTC1)
ENST00000560563.1:n.306T>C (ACTC1)
NM_005159.4:c.807T>C , LRG_388t1:c.807T>C (ACTC1) NP_005150.1:p.Ile269=
NR_120329.1:n.299+14660A>G (GJD2-DT)
NM_005159.5:c.807T>C (ACTC1) MANE Select NP_005150.1:p.Ile269=