Canonical Allele Identifier: CA489655409
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.35084613G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792412G>T , CM000677.2:g.34792412G>T GRCh38
NC_000015.9:g.35084613G>T , CM000677.1:g.35084613G>T GRCh37
NC_000015.8:g.32871905G>T NCBI36
NG_007553.1:g.8315C>A , LRG_388:g.8315C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.718C>A (ACTC1)
ENST00000290378.6:c.612C>A (ACTC1) MANE Select ENSP00000290378.4:p.Thr204=
ENST00000647798.1:n.706C>A (ACTC1)
ENST00000648556.1:n.769C>A (ACTC1)
ENST00000650163.1:n.692C>A (ACTC1)
ENST00000290378.4:c.612C>A (ACTC1) ENSP00000290378.4:p.Thr204=
ENST00000557860.1:n.302C>A (ACTC1)
ENST00000560563.1:n.111C>A (ACTC1)
NM_005159.4:c.612C>A , LRG_388t1:c.612C>A (ACTC1) NP_005150.1:p.Thr204=
NR_120329.1:n.299+14981G>T (GJD2-DT)
NM_005159.5:c.612C>A (ACTC1) MANE Select NP_005150.1:p.Thr204=