Canonical Allele Identifier: CA2169204522
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34790621T= , CM000677.2:g.34790621T= GRCh38
NC_000015.9:g.35082822T= , CM000677.1:g.35082822T= GRCh37
NC_000015.8:g.32870114T= NCBI36
NG_007553.1:g.10106A= , LRG_388:g.10106A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.1891-66A= (ACTC1)
ENST00000290378.6:c.991-66A= (ACTC1) MANE Select ENSP00000290378.4:n.991-66A=
ENST00000647798.1:n.1085-66A= (ACTC1)
ENST00000650163.1:n.1071-66A= (ACTC1)
ENST00000290378.4:c.991-66A= (ACTC1) ENSP00000290378.4:n.991-66A=
NM_005159.4:c.991-66A= , LRG_388t1:c.991-66A= (ACTC1) NP_005150.1:n.991-66A=
NR_120329.1:n.299+13190T= (GJD2-DT)
NM_005159.5:c.991-66A= (ACTC1) MANE Select NP_005150.1:n.991-66A=