Canonical Allele Identifier: CA2169205716
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34791259T= , CM000677.2:g.34791259T= GRCh38
NC_000015.9:g.35083460T= , CM000677.1:g.35083460T= GRCh37
NC_000015.8:g.32870752T= NCBI36
NG_007553.1:g.9468A= , LRG_388:g.9468A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560563.2:n.1745A= (ACTC1)
ENST00000290378.6:c.845A= (ACTC1) MANE Select ENSP00000290378.4:p.Asn282=
ENST00000647798.1:n.939A= (ACTC1)
ENST00000650163.1:n.925A= (ACTC1)
ENST00000290378.4:c.845A= (ACTC1) ENSP00000290378.4:p.Asn282=
ENST00000557860.1:n.535A= (ACTC1)
NM_005159.4:c.845A= , LRG_388t1:c.845A= (ACTC1) NP_005150.1:p.Asn282=
NR_120329.1:n.299+13828T= (GJD2-DT)
NM_005159.5:c.845A= (ACTC1) MANE Select NP_005150.1:p.Asn282=